A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951492



Internal ID35017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82971203..82975182hg38UCSC Ensembl
chr4:83892356..83896335hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464420
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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