A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891786



Internal ID19186182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38290160..38330246hg38UCSC Ensembl
Outerchr10:38290160..38330246hg38UCSC Ensembl
Innerchr10:38579088..38619174hg19UCSC Ensembl
Outerchr10:38579088..38619174hg19UCSC Ensembl
Innerchr10:38619094..38659180hg18UCSC Ensembl
Outerchr10:38619094..38659180hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3840087
hg1940087
hg1840087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782921
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891786
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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