A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542695



Internal ID21867050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100645812..100645812hg38UCSC Ensembl
chr4:101566969..101566969hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542695
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