A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010096



Internal ID74370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27770325..27776131hg38UCSC Ensembl
chr8:27627842..27633648hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg385807
hg195807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480676
Supporting Variants
Samples
Known GenesCCDC25, ESCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010096
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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