A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009799



Internal ID16303755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160118192..160158193hg38UCSC Ensembl
Innerchr4:161039344..161079345hg19UCSC Ensembl
Innerchr4:161258794..161298795hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3840002
hg1940002
hg1840002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595826
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)nssv1009799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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