A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202139



Internal ID20769179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99095980..99115724hg38UCSC Ensembl
chr1:99561536..99581280hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3819745
hg1919745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331448
Supporting Variants
Samples
Known GenesLOC100129620
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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