A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577015



Internal ID21769058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172551135..172551198hg38UCSC Ensembl
chr5:171978138..171978201hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577015
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