A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698060



Internal ID15088026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113339111..113340183hg38UCSC Ensembl
Innerchr9:116101391..116102463hg19UCSC Ensembl
Innerchr9:115141212..115142284hg18UCSC Ensembl
Innerchr9:113180945..113182017hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381073
hg191073
hg181073
hg171073
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521449
Supporting Variants
Samples
Known GenesWDR31
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698060
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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