A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983582



Internal ID56431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35259647..35259688hg38UCSC Ensembl
chr6:35227424..35227465hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983582
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002654


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