A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522597



Internal ID15103204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28724519..30074044hg38UCSC Ensembl
Innerchr15:28969665..30366247hg19UCSC Ensembl
Innerchr15:26768706..28153539hg18UCSC Ensembl
Innerchr15:26768706..28153539hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381349526
hg191396583
hg181384834
hg171384834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705987
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)nsv522597
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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