A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359561



Internal ID21017114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180026833..180027285hg38UCSC Ensembl
chr3:179744621..179745073hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100428
Samples
Known GenesPEX5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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