A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600765



Internal ID16388174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296257..361547hg38UCSC Ensembl
Innerchr6:296257..361547hg19UCSC Ensembl
Innerchr6:241257..306547hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3865291
hg1965291
hg1865291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10264n54
Supporting Variantsnssv1047573
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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