A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992615



Internal ID20559655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70303296..70308780hg38UCSC Ensembl
chr11:70149402..70154886hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385485
hg195485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470617
Supporting Variants
Samples
Known GenesPPFIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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