A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1061125



Internal ID15914311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61891075..62217609hg38UCSC Ensembl
Innerchr6:62600980..62927514hg19UCSC Ensembl
Innerchr6:62658939..62985473hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38326535
hg19326535
hg18326535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603316
Supporting Variants
Samples
Known GenesKHDRBS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1061125
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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