A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459663



Internal ID21117216
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 StatusM
Merged Variants
Supporting Variantsnssv17986917
Samples
Known GenesNXPE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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