A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559824



Internal ID16347233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95617401..95618064hg38UCSC Ensembl
Innerchr12:96011177..96011840hg19UCSC Ensembl
Innerchr12:94535308..94535971hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38664
hg19664
hg18664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2802n54
Supporting Variantsnssv800814, nssv800816, nssv800815
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559824
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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