A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739402



Internal ID18690997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48782315..49152740hg38UCSC Ensembl
Innerchr4:48784332..49154757hg19UCSC Ensembl
Innerchr4:48479089..48849514hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38370426
hg19370426
hg18370426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011910
Supporting Variants
Samples
Known GenesCWH43, OCIAD1, OCIAD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739402
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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