A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739512



Internal ID20515485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45418741..45428909hg38UCSC Ensembl
chr13:45992876..46003044hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3810169
hg1910169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739512
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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