A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996680



Internal ID16290636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42695536..42706918hg38UCSC Ensembl
Innerchr4:42697553..42708935hg19UCSC Ensembl
Innerchr4:42392310..42403692hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3811383
hg1911383
hg1811383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594059
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)nssv996680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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