A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890968



Internal ID19185364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156042514..156352109hg38UCSC Ensembl
Outerchr6:156042514..156352109hg38UCSC Ensembl
Innerchr6:156363648..156673243hg19UCSC Ensembl
Outerchr6:156363648..156673243hg19UCSC Ensembl
Innerchr6:156405340..156714935hg18UCSC Ensembl
Outerchr6:156405340..156714935hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38309596
hg19309596
hg18309596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796828
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890968
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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