A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522370



Internal ID15449663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22229500..22264963hg38UCSC Ensembl
Innerchr1:22555993..22591456hg19UCSC Ensembl
Innerchr1:22428580..22464043hg18UCSC Ensembl
Innerchr1:22301299..22336762hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3835464
hg1935464
hg1835464
hg1735464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695150
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522370
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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