A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526362



Internal ID15453655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10773858..10790580hg38UCSC Ensembl
Innerchr9:10773858..10790580hg19UCSC Ensembl
Innerchr9:10763858..10780580hg18UCSC Ensembl
Innerchr9:10763858..10780580hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3816723
hg1916723
hg1816723
hg1716723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702655
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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