A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893824



Internal ID19184644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176872905..176935352hg38UCSC Ensembl
Outerchr3:176872905..176935352hg38UCSC Ensembl
Innerchr3:176590693..176653140hg19UCSC Ensembl
Outerchr3:176590693..176653140hg19UCSC Ensembl
Innerchr3:178073387..178135834hg18UCSC Ensembl
Outerchr3:178073387..178135834hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3862448
hg1962448
hg1862448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792411
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893824
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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