A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687646



Internal ID15424298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127162373..127213326hg38UCSC Ensembl
Innerchr9:129924652..129975605hg19UCSC Ensembl
Innerchr9:128964473..129015426hg18UCSC Ensembl
Innerchr9:127004206..127055159hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3850954
hg1950954
hg1850954
hg1750954
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)nssv687646
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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