A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463499



Internal ID21121052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34939701..34943300hg38UCSC Ensembl
chr11:34961248..34964847hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194050
Samples
Known GenesMIR1343, PDHX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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