A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075792



Internal ID15928978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709839..164800526hg38UCSC Ensembl
Innerchr6:165130872..165214015hg19UCSC Ensembl
Innerchr6:165050862..165134005hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3890688
hg1983144
hg1883144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605238
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075792
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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