A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515949



Internal ID15443006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32748367..32753511hg38UCSC Ensembl
Innerchr9:32748365..32753509hg19UCSC Ensembl
Innerchr9:32738365..32743509hg18UCSC Ensembl
Innerchr9:32738365..32743509hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385145
hg195145
hg185145
hg175145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv484n21
Supporting Variantsnssv665424, nssv660205, nssv679261, nssv681148, nssv666190
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515949
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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