A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152579



Internal ID15527065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3411482..3447925hg38UCSC Ensembl
Innerchr4:3413209..3449652hg19UCSC Ensembl
Innerchr4:3383007..3419450hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3836444
hg1936444
hg1836444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593452
Supporting Variants
SamplesHGDP00330
Known GenesHGFAC, RGS12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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