A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471592



Internal ID21129145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84411081..84454372hg38UCSC Ensembl
chr11:84122124..84165415hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843292
hg1943292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179872
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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