A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458040



Internal ID21115593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44617297..44619501hg38UCSC Ensembl
chr11:44638847..44641051hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196330
Samples
Known GenesCD82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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