A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519131



Internal ID15446424
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696611
Samples
Known GenesTNC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519131
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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