A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639398



Internal ID18937679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121885073..121927811hg38UCSC Ensembl
Innerchr4:122806228..122848966hg19UCSC Ensembl
Innerchr4:123025678..123068416hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3842739
hg1942739
hg1842739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014729
Supporting Variants
Samples
Known GenesTRPC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639398
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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