A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518662



Internal ID20892023
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 StatusM
Merged Variants
Supporting Variantsnssv18193260
Samples
Known GenesB3GNTL1, METRNL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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