A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659925



Internal ID15396577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161082472hg38UCSC Ensembl
Innerchr4:161945302..162003624hg19UCSC Ensembl
Innerchr4:162164752..162223074hg18UCSC Ensembl
Innerchr4:162302907..162361229hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3858323
hg1958323
hg1858323
hg1758323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515755
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659925
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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