A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977150



Internal ID22752085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51070888..51070888hg38UCSC Ensembl
chr13:51645024..51645024hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977150
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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