A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375211



Internal ID21032764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95738101..95750200hg38UCSC Ensembl
chr3:95456945..95469044hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375211
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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