A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600772



Internal ID16388181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:312247..381918hg38UCSC Ensembl
Innerchr6:312247..381918hg19UCSC Ensembl
Innerchr6:257247..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3869672
hg1969672
hg1869672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10264n54
Supporting Variantsnssv1047581, nssv1047580
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600772
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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