A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779801



Internal ID19169801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3819022..3826906hg38UCSC Ensembl
Innerchr10:3861214..3869098hg19UCSC Ensembl
Innerchr10:3851214..3859098hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg387885
hg197885
hg187885
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891741
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779801
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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