A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705502



Internal ID15442154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130396541..130400192hg38UCSC Ensembl
Innerchr9:133271928..133275579hg19UCSC Ensembl
Innerchr9:132261749..132265400hg18UCSC Ensembl
Innerchr9:130301482..130305133hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383652
hg193652
hg183652
hg173652
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528828
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705502
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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