A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527255



Internal ID15107862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28754022..30074044hg38UCSC Ensembl
Innerchr15:28999168..30366247hg19UCSC Ensembl
Innerchr15:26798209..28153539hg18UCSC Ensembl
Innerchr15:26798209..28153539hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381320023
hg191367080
hg181355331
hg171355331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703659
Samples
Known GenesAPBA2, FAM189A1, GOLGA6L7P, LOC100289656, LOC646278, NDNL2, TJP1, WHAMMP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527255
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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