A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986917



Internal ID20553957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114531601..114536000hg38UCSC Ensembl
chr11:114402323..114406722hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459663
Supporting Variants
Samples
Known GenesNXPE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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