A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530786



Internal ID20904147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44663645..44672619hg38UCSC Ensembl
chr19:45166912..45175891hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg388975
hg198980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048188
Samples
Known GenesCEACAM19, PVR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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