A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1006137



Internal ID16300093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121712380..121799844hg38UCSC Ensembl
Innerchr4:122633535..122720999hg19UCSC Ensembl
Innerchr4:122852985..122940449hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3887465
hg1987465
hg1887465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595357
Supporting Variants
Samples
Known GenesPP12613, TMEM155
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1006137
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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