A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188018



Internal ID20755058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10584988..10606307hg38UCSC Ensembl
chr17:10488305..10509624hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3821320
hg1921320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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