A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531870



Internal ID21856226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17054973..17054973hg38UCSC Ensembl
chr1:17381468..17381468hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531870
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