A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119921



Internal ID20686961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82991601..82998300hg38UCSC Ensembl
chr4:83912754..83919453hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388283
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00741


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