A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655598



Internal ID15045564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127263077..127273883hg38UCSC Ensembl
Innerchr9:130025356..130036162hg19UCSC Ensembl
Innerchr9:129065177..129075983hg18UCSC Ensembl
Innerchr9:127104910..127115716hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810807
hg1910807
hg1810807
hg1710807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516966
Supporting Variants
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655598
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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