A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422150



Internal ID22480020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153318479..153321878hg38UCSC Ensembl
chr4:154239631..154243030hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895086
Supporting Variants
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422150
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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