A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524809



Internal ID20898170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17359282..17361656hg38UCSC Ensembl
chr19:17470091..17472465hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382375
hg192375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045178
Samples
Known GenesPLVAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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