A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696120



Internal ID15432772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115699544..115835558hg38UCSC Ensembl
Innerchr9:118461823..118597837hg19UCSC Ensembl
Innerchr9:117501644..117637658hg18UCSC Ensembl
Innerchr9:115541377..115677391hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38136015
hg19136015
hg18136015
hg17136015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518670
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696120
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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