A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152578



Internal ID15530681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3411482..3444385hg38UCSC Ensembl
Innerchr4:3413209..3446112hg19UCSC Ensembl
Innerchr4:3383007..3415910hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3832904
hg1932904
hg1832904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593451
Supporting Variants
SamplesHGDP00975
Known GenesHGFAC, RGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152578
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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