A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596563



Internal ID21788606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70553932..70557803hg38UCSC Ensembl
chr10:72313688..72317559hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383872
hg193872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017550
Supporting Variants
Samples
Known GenesPALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596563
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