A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410396



Internal ID22468266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140565830..140565830hg38UCSC Ensembl
chr4:141486984..141486984hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954100
Supporting Variants
Samples
Known GenesUCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410396
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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