A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032908



Internal ID19122130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131507980..131626271hg38UCSC Ensembl
Innerchr4:132429135..132547426hg19UCSC Ensembl
Innerchr4:132648585..132766876hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38118292
hg19118292
hg18118292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5390n100
Supporting Variantsnssv3639483
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032908
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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