A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521747



Internal ID15449040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107656293..107678832hg38UCSC Ensembl
Innerchr9:110418574..110441113hg19UCSC Ensembl
Innerchr9:109458395..109480934hg18UCSC Ensembl
Innerchr9:107498129..107520668hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3822540
hg1922540
hg1822540
hg1722540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694513
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521747
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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