A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988331



Internal ID59649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90367838..90367838hg38UCSC Ensembl
chr6:91077557..91077557hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988331
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.038341


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