A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515660



Internal ID15096267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29250908..29272431hg38UCSC Ensembl
Innerchr15:29543112..29564635hg19UCSC Ensembl
Innerchr15:27330404..27351927hg18UCSC Ensembl
Innerchr15:27330404..27351927hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3821524
hg1921524
hg1821524
hg1721524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669926, nssv678067, nssv674085, nssv665492, nssv680961, nssv671370, nssv681372, nssv671046, nssv669149, nssv687493, nssv664278, nssv685292
Samples
Known GenesFAM189A1, NDNL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515660
Frequency
Sample Size2026
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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