A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515900



Internal ID15442957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78432975..78442493hg38UCSC Ensembl
Innerchr9:81047891..81057409hg19UCSC Ensembl
Innerchr9:80237711..80247229hg18UCSC Ensembl
Innerchr9:78277445..78286963hg17UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389519
hg199519
hg189519
hg179519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655945, nssv665195, nssv677934
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515900
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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