A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671370



Internal ID15061336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29258615..29272431hg38UCSC Ensembl
Innerchr15:29550819..29564635hg19UCSC Ensembl
Innerchr15:27338111..27351927hg18UCSC Ensembl
Innerchr15:27338111..27351927hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3813817
hg1913817
hg1813817
hg1713817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515660
Supporting Variants
Samples
Known GenesFAM189A1, NDNL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671370
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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