A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789941



Internal ID19165670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22775773..22821868hg38UCSC Ensembl
Innerchr10:23064702..23110797hg19UCSC Ensembl
Innerchr10:23104708..23150803hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3846096
hg1946096
hg1846096
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891776
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789941
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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