A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686686



Internal ID15423338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31778861..31787274hg38UCSC Ensembl
Innerchr5:31778968..31787381hg19UCSC Ensembl
Innerchr5:31814725..31823138hg18UCSC Ensembl
Innerchr5:31814725..31823138hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388414
hg198414
hg188414
hg178414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515692
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686686
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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