A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109624



Internal ID22018857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33757599..33757599hg38UCSC Ensembl
chr19:34248504..34248504hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634723
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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