A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1064421



Internal ID15917607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73956843..74234744hg38UCSC Ensembl
Innerchr6:74666559..74944460hg19UCSC Ensembl
Innerchr6:74723279..75001180hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38277902
hg19277902
hg18277902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603733
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)nssv1064421
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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