A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007538



Internal ID72660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17771011..17959018hg38UCSC Ensembl
chr8:17628520..17816527hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38188008
hg19188008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479908
Supporting Variants
Samples
Known GenesFGL1, MTUS1, PCM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007538
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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