A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232998



Internal ID20800038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52853223..52988689hg38UCSC Ensembl
chr8:53765783..53901249hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38135467
hg19135467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434963
Supporting Variants
Samples
Known GenesNPBWR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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