A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696611



Internal ID15433263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115034707..115042388hg38UCSC Ensembl
Innerchr9:117796986..117804667hg19UCSC Ensembl
Innerchr9:116836807..116844488hg18UCSC Ensembl
Innerchr9:114876540..114884221hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg387682
hg197682
hg187682
hg177682
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519131
Supporting Variants
Samples
Known GenesTNC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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