A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067242



Internal ID15920428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78981458..79018611hg38UCSC Ensembl
Innerchr6:79691175..79728328hg19UCSC Ensembl
Innerchr6:79747894..79785047hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3837154
hg1937154
hg1837154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604051
Supporting Variants
Samples
Known GenesPHIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067242
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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