A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742777



Internal ID20518762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31369521..31371821hg38UCSC Ensembl
chr13:31943658..31945958hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742777
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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