A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187362



Internal ID20754402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73962984..74017161hg38UCSC Ensembl
chr10:75722742..75776919hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3854178
hg1954178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454302
Supporting Variants
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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