A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119919



Internal ID20686959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82989096..82992747hg38UCSC Ensembl
chr4:83910249..83913900hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg383652
hg193652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381575
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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