A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680446



Internal ID21202308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153724963..153725043hg38UCSC Ensembl
chr4:154646115..154646195hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809381
Supporting Variants
Samples
Known GenesRNF175
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680446
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.583333


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