A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464166



Internal ID21121719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124016553..124023991hg38UCSC Ensembl
chr11:123887260..123894698hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg387439
hg197439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987220
Samples
Known GenesOR10G9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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