A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524671



Internal ID15451964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136622988..136627649hg38UCSC Ensembl
Innerchr9:139517440..139522101hg19UCSC Ensembl
Innerchr9:138637261..138641922hg18UCSC Ensembl
Innerchr9:136793277..136797938hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384662
hg194662
hg184662
hg174662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700641
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524671
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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