A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601174



Internal ID16388583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26341073..26350710hg38UCSC Ensembl
Innerchr6:26341301..26350938hg19UCSC Ensembl
Innerchr6:26449280..26458917hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389638
hg199638
hg189638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051368
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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