A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570177



Internal ID21762220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159710680..159712772hg38UCSC Ensembl
chr6:160131712..160133804hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013828
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570177
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