A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181717



Internal ID20748757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43425784..43442706hg38UCSC Ensembl
chr10:43921232..43938154hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3816923
hg1916923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449410
Supporting Variants
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181717
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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