A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529026



Internal ID15456319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34743684..34819534hg38UCSC Ensembl
Innerchr9:34743681..34819531hg19UCSC Ensembl
Innerchr9:34733681..34809531hg18UCSC Ensembl
Innerchr9:34733681..34809531hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3875851
hg1975851
hg1875851
hg1775851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705737
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529026
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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