A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621010



Internal ID21813057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45672002..45672002hg38UCSC Ensembl
chr19:46175260..46175260hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106364
Supporting Variants
Samples
Known GenesGIPR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621010
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer