A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521117



Internal ID15448410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126496558..126522010hg38UCSC Ensembl
Innerchr9:129258837..129284289hg19UCSC Ensembl
Innerchr9:128298658..128324110hg18UCSC Ensembl
Innerchr9:126338391..126363843hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3825453
hg1925453
hg1825453
hg1725453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697796
Samples
Known GenesMVB12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521117
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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