A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522442



Internal ID15449735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163746573..163796035hg38UCSC Ensembl
Innerchr1:163715810..163765272hg19UCSC Ensembl
Innerchr1:161982434..162031896hg18UCSC Ensembl
Innerchr1:160447468..160496930hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3849463
hg1949463
hg1849463
hg1749463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705800
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522442
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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