A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523938



Internal ID20897299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5677066..5685512hg38UCSC Ensembl
chr19:5677077..5685523hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388447
hg198447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049366
Samples
Known GenesC19orf70, HSD11B1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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