A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572751



Internal ID21764794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2464236..2464725hg38UCSC Ensembl
chr6:2464470..2464959hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572751
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer