A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520323



Internal ID20893684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4463447..4470307hg38UCSC Ensembl
chr19:4463444..4470304hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386861
hg196861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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