A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422696



Internal ID22480566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152698608..152700807hg38UCSC Ensembl
chr4:153619760..153621959hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422696
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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