A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623730



Internal ID7010586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68852320..68864024hg38UCSC Ensembl
Innerchr10:68852366..68863979hg38UCSC Ensembl
Outerchr10:68852275..68864070hg38UCSC Ensembl
chr10:70612076..70623780hg19UCSC Ensembl
Innerchr10:70612122..70623735hg19UCSC Ensembl
Outerchr10:70612031..70623826hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3811705
hg1911705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13851588, essv13851582, essv13851583, essv13851574, essv13851570, essv13851580, essv13851578, essv13851584, essv13851587, essv13851576, essv13851572, essv13851589, essv13851579, essv13851592, essv13851585, essv13851577, essv13851571, essv13851573, essv13851593, essv13851575, essv13851590, essv13851591, essv13851586, essv13851581
SamplesHG02702, HG01066, HG02624, HG03082, HG02811, NA19315, HG03479, HG02634, HG03195, NA19159, HG03027, HG02757, NA18853, HG03046, NA18523, HG02759, HG03539, HG02983, HG03259, HG02982, HG01105, HG03445, HG02763, HG02465
Known GenesSTOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623730
Frequency
Sample Size2504
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer