A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618097



Internal ID7004980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95067153..95070097hg38UCSC Ensembl
Innerchr8:95067153..95070097hg38UCSC Ensembl
Outerchr8:95066965..95070236hg38UCSC Ensembl
chr8:96079381..96082325hg19UCSC Ensembl
Innerchr8:96079381..96082325hg19UCSC Ensembl
Outerchr8:96079193..96082464hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382945
hg192945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13261469, essv13261440, essv13261439, essv13261461, essv13261466, essv13261437, essv13261443, essv13261441, essv13261453, essv13261430, essv13261467, essv13261458, essv13261447, essv13261445, essv13261438, essv13261451, essv13261449, essv13261464, essv13261435, essv13261434, essv13261432, essv13261463, essv13261468, essv13261429, essv13261465, essv13261442, essv13261456, essv13261462, essv13261444, essv13261446, essv13261457, essv13261452, essv13261471, essv13261448, essv13261454, essv13261433, essv13261460, essv13261470, essv13261455, essv13261459, essv13261431, essv13261436, essv13261450
SamplesHG02610, HG02628, HG03057, HG03241, HG02852, NA19092, NA19190, NA19446, NA19764, HG02952, NA19138, NA19130, NA19923, NA19385, NA19471, HG03169, HG02716, HG02439, HG03054, HG03061, HG02554, HG02450, NA20126, HG03124, HG01390, HG03472, HG03388, NA20282, HG02586, HG01956, HG03028, NA18517, HG02317, NA20281, HG01089, NA19102, NA19711, HG03470, HG03401, HG02052, HG01883, NA19129, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618097
Frequency
Sample Size2504
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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