A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692279



Internal ID15428931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352335..57488840hg38UCSC Ensembl
Innerchr15:57644533..57781038hg19UCSC Ensembl
Innerchr15:55431825..55568330hg18UCSC Ensembl
Innerchr15:55431825..55568330hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38136506
hg19136506
hg18136506
hg17136506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516366
Supporting Variants
Samples
Known GenesCGNL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692279
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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