A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069734



Internal ID21978967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122761199..122761199hg38UCSC Ensembl
chr5:122096894..122096894hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069734
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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