A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373732



Internal ID22599401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20882127..20882127hg38UCSC Ensembl
chr13:21456266..21456266hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977231
Supporting Variants
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373732
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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