A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661459



Internal ID15398111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104051184..104072028hg38UCSC Ensembl
Innerchr9:106813465..106834309hg19UCSC Ensembl
Innerchr9:105853286..105874130hg18UCSC Ensembl
Innerchr9:103893020..103913864hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3820845
hg1920845
hg1820845
hg1720845
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516897
Supporting Variants
Samples
Known GenesMIR6130
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661459
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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