A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395749



Internal ID22453619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31577941..31577941hg38UCSC Ensembl
chr20:30165744..30165744hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395749
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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