A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798713



Internal ID19176399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123109117..123119667hg38UCSC Ensembl
Innerchr10:124868633..124879183hg19UCSC Ensembl
Innerchr10:124858623..124869173hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810551
hg1910551
hg1810551
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891894
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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