A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374396



Internal ID21031949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111113701..111153100hg38UCSC Ensembl
chr3:110832548..110871947hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3839400
hg1939400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207250
Samples
Known GenesPVRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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