A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668684



Internal ID15058650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:141576210..141624764hg38UCSC Ensembl
Innerchr5:140955777..141004331hg19UCSC Ensembl
Innerchr5:140935961..140984515hg18UCSC Ensembl
Innerchr5:140935961..140984515hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3848555
hg1948555
hg1848555
hg1748555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516495
Supporting Variants
Samples
Known GenesDIAPH1, HDAC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668684
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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