A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739565



Internal ID19037846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4047125..4058193hg38UCSC Ensembl
Innerchr3:4088809..4099877hg19UCSC Ensembl
Innerchr3:4063809..4074877hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3811069
hg1911069
hg1811069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002540
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)nssv3739565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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