A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073353



Internal ID21982586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17173356..17173356hg38UCSC Ensembl
chr8:17030865..17030865hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560385
Samples
Known GenesZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073353
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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