A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557761



Internal ID21882116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134717432..134719060hg38UCSC Ensembl
chr6:135038570..135040198hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381629
hg191629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557761
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