A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788350



Internal ID18826730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7698285..7742961hg38UCSC Ensembl
Innerchr10:7740248..7784924hg19UCSC Ensembl
Innerchr10:7780254..7824930hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3844677
hg1944677
hg1844677
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891752
Supporting Variants
Samples
Known GenesITIH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788350
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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