A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977611



Internal ID22752546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29701656..29701656hg38UCSC Ensembl
chr13:30275793..30275793hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977611
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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