A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528864



Internal ID20902225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3439930..3440763hg38UCSC Ensembl
chr19:3439928..3440761hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046226
Samples
Known GenesNFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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