A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478468



Internal ID18721422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:19427353..19449317hg38UCSC Ensembl
Innerchr1:19753847..19775811hg19UCSC Ensembl
Innerchr1:19626434..19648398hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821965
hg1921965
hg1821965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014816
Supporting Variants
Samples
Known GenesCAPZB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3478468
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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