A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983817



Internal ID56588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76821545..76844882hg38UCSC Ensembl
chr6:77531262..77554599hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3823338
hg1923338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983817
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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