A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987866



Internal ID20554906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1251888..1252188hg38UCSC Ensembl
chr11:1273118..1273418hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437584
Supporting Variants
Samples
Known GenesMUC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987866
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