A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202495



Internal ID20769535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23765143..23767333hg38UCSC Ensembl
chr1:24091633..24093823hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328640
Supporting Variants
Samples
Known GenesLOC100506963
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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