A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522020



Internal ID15102627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61813922..62052275hg38UCSC Ensembl
Innerchr1:62279594..62517947hg19UCSC Ensembl
Innerchr1:62052182..62290535hg18UCSC Ensembl
Innerchr1:61991615..62229968hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38238354
hg19238354
hg18238354
hg17238354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n21
Supporting Variantsnssv694789
Samples
Known GenesINADL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522020
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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