A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532238



Internal ID20905599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49530724..49536492hg38UCSC Ensembl
chr19:50033981..50039749hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385769
hg195769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047177
Samples
Known GenesRCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532238
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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