A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730725



Internal ID20506638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90314321..90314424hg38UCSC Ensembl
chr13:90966575..90966678hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730725
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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