A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695757



Internal ID15432409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37382102..37387221hg38UCSC Ensembl
Innerchr9:37382099..37387218hg19UCSC Ensembl
Innerchr9:37372099..37377218hg18UCSC Ensembl
Innerchr9:37372099..37377218hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg385120
hg195120
hg185120
hg175120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518327
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695757
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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