A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676706



Internal ID15413358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127166841..127198873hg38UCSC Ensembl
Innerchr9:129929120..129961152hg19UCSC Ensembl
Innerchr9:128968941..129000973hg18UCSC Ensembl
Innerchr9:127008674..127040706hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3832033
hg1932033
hg1832033
hg1732033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517522
Supporting Variants
Samples
Known GenesRALGPS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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