A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620653



Internal ID18918934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33999447..35826250hg38UCSC Ensembl
Innerchr4:34001069..35827872hg19UCSC Ensembl
Innerchr4:33677464..35504267hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381826804
hg191826804
hg181826804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011636
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)nssv3620653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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