A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3613636



Internal ID18911917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176165155..176196679hg38UCSC Ensembl
Innerchr3:175882943..175914467hg19UCSC Ensembl
Innerchr3:177365637..177397161hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3831525
hg1931525
hg1831525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005105
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3613636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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