A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212421



Internal ID20779461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111806281..111829210hg38UCSC Ensembl
chr5:111141978..111164907hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3822930
hg1922930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408571
Supporting Variants
Samples
Known GenesNREP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212421
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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