A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559851



Internal ID16347260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97648767..97668107hg38UCSC Ensembl
Innerchr12:98042545..98061885hg19UCSC Ensembl
Innerchr12:96566676..96586016hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3819341
hg1919341
hg1819341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800872
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559851
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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