A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060986



Internal ID18803517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36762121..36829244hg38UCSC Ensembl
Innerchr22:37158165..37225287hg19UCSC Ensembl
Innerchr22:35488111..35555233hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3867124
hg1967123
hg1867123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600870
Samples
Known GenesIFT27, PVALB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060986
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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