A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601053



Internal ID16388462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18401914..18404813hg38UCSC Ensembl
Innerchr6:18402145..18405044hg19UCSC Ensembl
Innerchr6:18510124..18513023hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382900
hg192900
hg182900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1050621
Samples
Known GenesRNF144B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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