A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782921



Internal ID19171256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38290160..38330246hg38UCSC Ensembl
Innerchr10:38579088..38619174hg19UCSC Ensembl
Innerchr10:38619094..38659180hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3840087
hg1940087
hg1840087
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891786
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782921
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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