A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067629



Internal ID21976862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170754158..170754158hg38UCSC Ensembl
chr5:170181162..170181162hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067629
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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