A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568333



Internal ID21760376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15103239..15103239hg38UCSC Ensembl
chr6:15103470..15103470hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568333
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