A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369782



Internal ID21027335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139931149..139949537hg38UCSC Ensembl
chr3:139649991..139668379hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3818389
hg1918389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093966
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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