A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226466



Internal ID20793506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38265201..38270900hg38UCSC Ensembl
chr8:38122719..38128418hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420095
Supporting Variants
Samples
Known GenesPPAPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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