A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628093



Internal ID21820140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35631140..35631209hg38UCSC Ensembl
chr17:33958159..33958228hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021240
Supporting Variants
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628093
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