A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517086



Internal ID15444379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22173037..22186354hg38UCSC Ensembl
Innerchr1:22499530..22512847hg19UCSC Ensembl
Innerchr1:22372117..22385434hg18UCSC Ensembl
Innerchr1:22244836..22258153hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3813318
hg1913318
hg1813318
hg1713318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661058, nssv669739, nssv679575, nssv687280, nssv671692, nssv664021, nssv677352, nssv653181, nssv653762, nssv664643, nssv665257, nssv683851, nssv656347, nssv663876, nssv682790, nssv684635, nssv671842, nssv666144, nssv676101, nssv663458, nssv682668
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517086
Frequency
Sample Size2026
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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