A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361162



Internal ID21018715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131488101..131489300hg38UCSC Ensembl
chr3:131206945..131208144hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094267
Samples
Known GenesMRPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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