A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987696



Internal ID16281652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1522203..1571637hg38UCSC Ensembl
Innerchr4:1523930..1573364hg19UCSC Ensembl
Innerchr4:1493470..1543447hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849435
hg1949435
hg1849978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593308
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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