A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739305



Internal ID20515278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101241792..101244071hg38UCSC Ensembl
chr13:101894143..101896422hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382280
hg192280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260926
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739305
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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