A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045163



Internal ID20612203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17207855..17216777hg38UCSC Ensembl
chr19:17318664..17327586hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg388923
hg198923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529933
Supporting Variants
Samples
Known GenesMYO9B, USE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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