A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360925



Internal ID21018478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123765024..123770321hg38UCSC Ensembl
chr3:123483871..123489168hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg385298
hg195298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095253
Samples
Known GenesMYLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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