A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638773



Internal ID21830820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14376413..14378452hg38UCSC Ensembl
chr21:15748734..15750773hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg382040
hg192040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042543
Supporting Variants
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638773
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