A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985017



Internal ID57401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87790394..87790394hg38UCSC Ensembl
chr6:88500112..88500112hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985017
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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