A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084571



Internal ID21993804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57675798..57675798hg38UCSC Ensembl
chr11:57443270..57443270hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382213
hg192213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578761
Samples
Known GenesZDHHC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084571
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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