A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119917



Internal ID20686957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82971200..82975182hg38UCSC Ensembl
chr4:83892353..83896335hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg383983
hg193983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391287
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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