A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573161



Internal ID21765204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157550339..157550396hg38UCSC Ensembl
chr6:157971371..157971428hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014632
Supporting Variants
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573161
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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