A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698211



Internal ID15088177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127263077..127290826hg38UCSC Ensembl
Innerchr9:130025356..130053105hg19UCSC Ensembl
Innerchr9:129065177..129092926hg18UCSC Ensembl
Innerchr9:127104910..127132659hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3827750
hg1927750
hg1827750
hg1727750
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521594
Supporting Variants
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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