A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517160



Internal ID15444453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111123414..111130683hg38UCSC Ensembl
Innerchr9:113885694..113892963hg19UCSC Ensembl
Innerchr9:112925515..112932784hg18UCSC Ensembl
Innerchr9:110965249..110972518hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg387270
hg197270
hg187270
hg177270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664885, nssv679159, nssv675155, nssv671279, nssv686094, nssv653896, nssv692661
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517160
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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