A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951463



Internal ID34996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82613809..82613911hg38UCSC Ensembl
chr4:83534962..83535064hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470013
Supporting Variants
Samples
Known GenesLINC00575
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951463
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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