A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529933



Internal ID20903294
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 StatusM
Merged Variants
Supporting Variantsnssv18045163
Samples
Known GenesMYO9B, USE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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