A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568549



Internal ID21760592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136957698..136957698hg38UCSC Ensembl
chr6:137278836..137278836hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568549
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