A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516723



Internal ID15444016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114562728..114576961hg38UCSC Ensembl
Innerchr9:117325008..117339241hg19UCSC Ensembl
Innerchr9:116364829..116379062hg18UCSC Ensembl
Innerchr9:114404562..114418795hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814234
hg1914234
hg1814234
hg1714234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670458, nssv677253, nssv689848, nssv688250, nssv682633
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516723
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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