A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519369



Internal ID15099976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33134619..33283163hg38UCSC Ensembl
Innerchr9:33134617..33283161hg19UCSC Ensembl
Innerchr9:33124617..33273161hg18UCSC Ensembl
Innerchr9:33124617..33273161hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38148545
hg19148545
hg18148545
hg17148545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655702, nssv660858
Samples
Known GenesB4GALT1, BAG1, CHMP5, LOC101929639, SPINK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519369
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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