A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618007



Internal ID21810054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55798373..56007565hg38UCSC Ensembl
chr19:56309739..56518931hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38209193
hg19209193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044653
Supporting Variants
Samples
Known GenesNLRP11, NLRP13, NLRP4, NLRP5, NLRP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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