A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522244



Internal ID15449537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88017880..88038687hg38UCSC Ensembl
Innerchr1:88483563..88504370hg19UCSC Ensembl
Innerchr1:88256151..88276958hg18UCSC Ensembl
Innerchr1:88195584..88216391hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3820808
hg1920808
hg1820808
hg1720808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695024
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522244
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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