A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992614



Internal ID20559654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70297225..70298984hg38UCSC Ensembl
chr11:70143331..70145090hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381760
hg191760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465659
Supporting Variants
Samples
Known GenesPPFIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992614
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