A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634723



Internal ID21826770
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 StatusS
Merged Variantsnsv6109624
Supporting Variants
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634723
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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