A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567150



Internal ID21759193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157552335..157552335hg38UCSC Ensembl
chr6:157973367..157973367hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063879
Supporting Variants
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567150
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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