A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526600



Internal ID15453893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133001900..133005806hg38UCSC Ensembl
Innerchr9:135877287..135881193hg19UCSC Ensembl
Innerchr9:134867108..134871014hg18UCSC Ensembl
Innerchr9:132906841..132910747hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383907
hg193907
hg183907
hg173907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702920
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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