A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787293



Internal ID19163763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56791607..56820575hg38UCSC Ensembl
Innerchr10:58551367..58580335hg19UCSC Ensembl
Innerchr10:58221373..58250341hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3828969
hg1928969
hg1828969
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891825
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787293
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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