A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624691



Internal ID7011541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118465594..118466839hg38UCSC Ensembl
Innerchr10:118465594..118466839hg38UCSC Ensembl
Outerchr10:118465073..118467114hg38UCSC Ensembl
chr10:120225106..120226351hg19UCSC Ensembl
Innerchr10:120225106..120226351hg19UCSC Ensembl
Outerchr10:120224585..120226626hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946652, essv13946653, essv13946656, essv13946660, essv13946636, essv13946648, essv13946643, essv13946651, essv13946669, essv13946655, essv13946667, essv13946659, essv13946639, essv13946668, essv13946662, essv13946641, essv13946649, essv13946661, essv13946665, essv13946650, essv13946642, essv13946664, essv13946654, essv13946666, essv13946646, essv13946637, essv13946640, essv13946645, essv13946638, essv13946644, essv13946657, essv13946663, essv13946658, essv13946647
SamplesHG03559, HG01462, HG03548, NA19378, NA12045, NA19098, NA19379, HG02562, NA19385, HG03225, NA18864, NA19209, HG02715, HG03132, HG01889, HG03202, NA19395, HG02568, HG02484, NA19401, HG03461, HG03437, NA19454, HG02923, NA19835, HG02274, HG03473, NA19475, NA19818, NA19143, NA19117, HG03313, HG02646, HG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624691
Frequency
Sample Size2504
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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