A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373525



Internal ID22599194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40473014..40473014hg38UCSC Ensembl
chr13:41047151..41047151hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975958
Supporting Variants
Samples
Known GenesLINC00598
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373525
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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