A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523327



Internal ID20896688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1263737..1264553hg38UCSC Ensembl
chr19:1263736..1264552hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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