A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179952



Internal ID20746992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25014001..25299300hg38UCSC Ensembl
chr11:25035547..25320846hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38285300
hg19285300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448808
Supporting Variants
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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