A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666613



Internal ID9932718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66025364..66025791hg38UCSC Ensembl
chr7:65490351..65490778hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5532585, essv5621510, essv5806821, essv6166717, essv6559725, essv5730008, essv5768296, essv5933182, essv6140951, essv6129148, essv5893260, essv6278106, essv6576282, essv6467201, essv6233915, essv6193253, essv5439447, essv6315859, essv6294932, essv6000706, essv5672042, essv6007184, essv5909332, essv5770279, essv6309167, essv5617171, essv6407881, essv5880339, essv5570346, essv6443685, essv5808311, essv5926856, essv6088887, essv6135470, essv5804264, essv6376355, essv6114251, essv6289746, essv6529662, essv6181936, essv6296038, essv6106605, essv5559268, essv5498073
SamplesNA19700, NA11931, NA19005, NA18519, NA18489, NA19448, NA18942, HG00736, NA19384, NA19130, NA19404, HG01080, NA12156, NA18868, NA19137, NA20340, NA19239, NA19451, NA19210, NA19455, NA18871, NA18976, HG01102, NA19461, NA18532, NA19452, NA18523, NA19160, NA18570, NA19375, NA19147, NA19435, NA19240, NA19311, HG01342, NA19818, NA19376, NA19398, NA20334, NA19129, NA19312, HG01125, NA18968, NA19153
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666613
Frequency
Sample Size1151
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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