A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520614



Internal ID20893975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17374430..17375992hg38UCSC Ensembl
chr19:17485239..17486801hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045180
Samples
Known GenesPLVAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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