A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363827



Internal ID22589496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101099062..101099062hg38UCSC Ensembl
chr13:101751413..101751413hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976271
Supporting Variants
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363827
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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