A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456167



Internal ID21113720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46871250..46871903hg38UCSC Ensembl
chr11:46892801..46893454hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991116
Samples
Known GenesLRP4, LRP4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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