A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367050



Internal ID21024603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136187426..136188476hg38UCSC Ensembl
chr3:135906268..135907318hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094919
Samples
Known GenesMSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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