A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559229



Internal ID16346638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69895940..69896929hg38UCSC Ensembl
Innerchr12:70289720..70290709hg19UCSC Ensembl
Innerchr12:68575987..68576976hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38990
hg19990
hg18990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2684n54
Supporting Variantsnssv797692
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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