A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016683



Internal ID78778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105466986..105467087hg38UCSC Ensembl
chr8:106479214..106479315hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142203
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016683
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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