A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626281



Internal ID21818328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3649523..3649523hg38UCSC Ensembl
chr19:3649521..3649521hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104201
Supporting Variants
Samples
Known GenesPIP5K1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626281
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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