A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623727



Internal ID7010583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68799678..68803155hg38UCSC Ensembl
Innerchr10:68800178..68802655hg38UCSC Ensembl
Outerchr10:68798678..68804155hg38UCSC Ensembl
chr10:70559435..70562912hg19UCSC Ensembl
Innerchr10:70559935..70562412hg19UCSC Ensembl
Outerchr10:70558435..70563912hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383478
hg193478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13851540, essv13851556, essv13851553, essv13851548, essv13851564, essv13851541, essv13851544, essv13851547, essv13851545, essv13851549, essv13851561, essv13851559, essv13851543, essv13851565, essv13851555, essv13851558, essv13851563, essv13851560, essv13851542, essv13851557, essv13851550, essv13851551, essv13851554, essv13851539, essv13851546, essv13851552, essv13851562
SamplesNA19028, HG02702, HG01066, HG02624, HG03082, HG02811, NA19315, HG03479, HG02634, HG03195, NA19159, HG03027, HG02757, HG03046, NA18523, NA18909, HG02759, HG03539, HG02546, HG02983, HG03259, HG02982, HG01105, HG03445, HG02763, HG02855, HG02465
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623727
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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