A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801953



Internal ID16095909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109713678..109713866hg38UCSC Ensembl
Innerchr12:110151483..110151671hg19UCSC Ensembl
Innerchr12:108635866..108636054hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38189
hg19189
hg18189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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