A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474701



Internal ID21132254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128519787..128520491hg38UCSC Ensembl
chr11:128389682..128390386hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987484
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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