A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533641



Internal ID20907002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41444140..41448919hg38UCSC Ensembl
chr19:41950045..41954824hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384780
hg194780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048083
Samples
Known GenesC19orf69
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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