A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688354



Internal ID15425006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127166841..127205859hg38UCSC Ensembl
Innerchr9:129929120..129968138hg19UCSC Ensembl
Innerchr9:128968941..129007959hg18UCSC Ensembl
Innerchr9:127008674..127047692hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3839019
hg1939019
hg1839019
hg1739019
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)nssv688354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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