A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458171



Internal ID21115724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114490737..114538506hg38UCSC Ensembl
chr11:114361459..114409228hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3847770
hg1947770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986913
Samples
Known GenesNXPE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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