A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048308



Internal ID100077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203051..73203990hg38UCSC Ensembl
chr11:72914096..72915035hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.028099


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