A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992037



Internal ID21901380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14177704..14178345hg38UCSC Ensembl
chr3:14219204..14219845hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546311
Samples
Known GenesXPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992037
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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