A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660161



Internal ID9926266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1664480..1668086hg38UCSC Ensembl
Outerchr7:1664109..1668456hg38UCSC Ensembl
Innerchr7:1704116..1707722hg19UCSC Ensembl
Outerchr7:1703745..1708092hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1178e199
Supporting Variantsessv6267105, essv5795814, essv6221911, essv5672141, essv6098523, essv5998363, essv5650341, essv5598146, essv6087924, essv6466242, essv6228067, essv5616548, essv5953588, essv5625519, essv6469313, essv5621374, essv5538231, essv5874809, essv6102339, essv6082672, essv5494862, essv5956661, essv5922963, essv6573432, essv6167038, essv5713451, essv6026979, essv5571480, essv5491496, essv5544180, essv6100539, essv5542676, essv5861688, essv5410207, essv6287364, essv5496352, essv5826408, essv6201811, essv5679105, essv5721487, essv5818566, essv6130051, essv5975477, essv5988756, essv5995281, essv5622914, essv5686846, essv6318995, essv6214729, essv6287269, essv5809126, essv6053956, essv6519282, essv6459453, essv5963787, essv5982123, essv5636971, essv5397981, essv5729109, essv5430448, essv5464082, essv6534538, essv5712814, essv5594650, essv6306169
SamplesNA19394, NA19397, NA19466, NA19399, NA19332, NA19350, NA19359, NA19355, NA19393, NA19377, NA19443, NA19446, NA19374, NA19396, NA19381, NA19373, NA19382, NA19315, NA19448, NA19457, NA19313, NA19384, NA19383, NA19372, NA19371, NA19471, NA19317, NA19445, NA19451, NA19462, NA19347, NA19391, NA19455, NA19461, NA19449, NA19453, NA19338, NA19452, NA19469, NA19436, NA19401, NA19375, NA19440, NA19434, NA19473, NA19435, NA19444, NA19334, NA19439, NA19470, NA19311, NA19467, NA19360, NA19398, NA19438, NA19472, NA19468, NA19474, NA19430, NA19316, NA19312, NA19463, NA19429, NA19346, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660161
Frequency
Sample Size1151
Observed Gain0
Observed Loss65
Observed Complex0
Frequencyn/a


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