A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951422



Internal ID34974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82155381..82179381hg38UCSC Ensembl
chr4:83076534..83100534hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3824001
hg1924001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951422
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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