A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988992



Internal ID20556032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2422165..2425318hg38UCSC Ensembl
chr11:2443395..2446548hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440391
Supporting Variants
Samples
Known GenesTRPM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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