A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209998



Internal ID20777038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52832609..52855968hg38UCSC Ensembl
chr3:52866625..52889984hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3823360
hg1923360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361280
Supporting Variants
Samples
Known GenesMIR8064, MUSTN1, TMEM110, TMEM110-MUSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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