A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679572



Internal ID15416224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113641805..113643195hg38UCSC Ensembl
Innerchr9:116404085..116405475hg19UCSC Ensembl
Innerchr9:115443906..115445296hg18UCSC Ensembl
Innerchr9:113483639..113485029hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381391
hg191391
hg181391
hg171391
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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