A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv787111



Internal ID16081067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:6134991..6149268hg38UCSC Ensembl
Innerchr12:6244157..6258434hg19UCSC Ensembl
Innerchr12:6114418..6128695hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3814278
hg1914278
hg1814278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557220
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)nssv787111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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