A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992192



Internal ID20559232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5250314..5255480hg38UCSC Ensembl
chr11:5271544..5276710hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385167
hg195167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436512
Supporting Variants
Samples
Known GenesHBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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