A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260775



Internal ID20469993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73276566..73276623hg38UCSC Ensembl
chr2:73503694..73503751hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260775
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer