A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152617



Internal ID15879048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7168835..7190053hg38UCSC Ensembl
Innerchr4:7170562..7191780hg19UCSC Ensembl
Innerchr4:7221463..7242681hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3821219
hg1921219
hg1821219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593562
Supporting Variants
SamplesHGDP01300
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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