A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361280



Internal ID21018833
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 StatusM
Merged Variants
Supporting Variantsnssv18209998
Samples
Known GenesMIR8064, MUSTN1, TMEM110, TMEM110-MUSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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