A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631051



Internal ID21823098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40583170..40583170hg38UCSC Ensembl
chr19:41089076..41089076hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101107
Supporting Variants
Samples
Known GenesSHKBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631051
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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