A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619670



Internal ID21811717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46945542..46947456hg38UCSC Ensembl
chr17:45022908..45024822hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619670
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