A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009754



Internal ID16303710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156447839..156520489hg38UCSC Ensembl
Innerchr4:157368991..157441641hg19UCSC Ensembl
Innerchr4:157588441..157661091hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3872651
hg1972651
hg1872651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595802
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)nssv1009754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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