A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536978



Internal ID21861333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231697391..231697478hg38UCSC Ensembl
chr2:232562101..232562188hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536978
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