A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1048755



Internal ID15901941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5426032..5511381hg38UCSC Ensembl
Innerchr6:5426265..5511614hg19UCSC Ensembl
Innerchr6:5371264..5456613hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3885350
hg1985350
hg1885350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600886
Supporting Variants
Samples
Known GenesFARS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1048755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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