A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365005



Internal ID21022558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177449414..177454934hg38UCSC Ensembl
chr3:177167202..177172722hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385521
hg195521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099699
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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