A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371360



Internal ID21028913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123682206..123689442hg38UCSC Ensembl
chr3:123401053..123408289hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg387237
hg197237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095247
Samples
Known GenesMYLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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