A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980977



Internal ID54695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11482169..11482176hg38UCSC Ensembl
chr6:11482402..11482409hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980977
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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