A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520876



Internal ID20894237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38306969..38314174hg38UCSC Ensembl
chr19:38797609..38804814hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387206
hg197206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047586
Samples
Known GenesYIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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