A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152594



Internal ID15876297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6254762..6301627hg38UCSC Ensembl
Innerchr4:6256489..6303354hg19UCSC Ensembl
Innerchr4:6307390..6354255hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3846866
hg1946866
hg1846866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593496
Supporting Variants
SamplesHGDP00817
Known GenesWFS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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