A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700646



Internal ID18652241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34786068..34884653hg38UCSC Ensembl
Innerchr1:35251669..35350254hg19UCSC Ensembl
Innerchr1:35024256..35122841hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3898586
hg1998586
hg1898586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012995
Supporting Variants
Samples
Known GenesDLGAP3, GJA4, GJB3, SMIM12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3700646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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