A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927882



Internal ID22703115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44243701..44245599hg38UCSC Ensembl
chr13:44817837..44819735hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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