A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474723



Internal ID21132276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79680701..79685500hg38UCSC Ensembl
chr11:79391745..79396544hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1235n223
Supporting Variantsnssv17994249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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