A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944979



Internal ID22720451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44704637..44710506hg38UCSC Ensembl
chr13:45278773..45284642hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg385870
hg195870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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