A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992875



Internal ID20559915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71501700..71504676hg38UCSC Ensembl
chr11:71212746..71215722hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00382


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