A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473709



Internal ID21131262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123339629..123558092hg38UCSC Ensembl
chr11:123210337..123428800hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38218464
hg19218464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194600
Samples
Known GenesGRAMD1B, MIR4493
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473709
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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