A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193260



Internal ID20760300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82959988..83185648hg38UCSC Ensembl
chr17:80917864..81133417hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38225661
hg19215554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518662
Supporting Variants
Samples
Known GenesB3GNTL1, METRNL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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