A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1007632



Internal ID16301588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135644754..135721005hg38UCSC Ensembl
Innerchr4:136565909..136642160hg19UCSC Ensembl
Innerchr4:136785359..136861610hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3876252
hg1976252
hg1876252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595515
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)nssv1007632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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