A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367264



Internal ID21024817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177489351..177489727hg38UCSC Ensembl
chr3:177207139..177207515hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099704
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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