A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891784



Internal ID19186180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36800190..36808001hg38UCSC Ensembl
Outerchr10:36800190..36808001hg38UCSC Ensembl
Innerchr10:37089118..37096929hg19UCSC Ensembl
Outerchr10:37089118..37096929hg19UCSC Ensembl
Innerchr10:37129124..37136935hg18UCSC Ensembl
Outerchr10:37129124..37136935hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg387812
hg197812
hg187812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800335
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891784
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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