A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009634



Internal ID16303590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155528678..155571831hg38UCSC Ensembl
Innerchr4:156449830..156492983hg19UCSC Ensembl
Innerchr4:156669280..156712433hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3843154
hg1943154
hg1843154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595755
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)nssv1009634
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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