A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120774



Internal ID20687814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94593401..94602300hg38UCSC Ensembl
chr4:95514552..95523451hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375707
Supporting Variants
Samples
Known GenesPDLIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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