A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063792



Internal ID21973025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157550335..157550335hg38UCSC Ensembl
chr6:157971367..157971367hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570933
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063792
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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