A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604606



Internal ID16392015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125860810..125865498hg38UCSC Ensembl
Innerchr6:126181956..126186644hg19UCSC Ensembl
Innerchr6:126223649..126228337hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg384689
hg194689
hg184689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10926n54
Supporting Variantsnssv1072406, nssv1072409, nssv1072410, nssv1072408, nssv1072407
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604606
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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