A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072402



Internal ID15925588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125860810..125864420hg38UCSC Ensembl
Innerchr6:126181956..126185566hg19UCSC Ensembl
Innerchr6:126223649..126227259hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg383611
hg193611
hg183611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604604
Supporting Variants
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072402
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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