A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462772



Internal ID21120325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59139801..59182500hg38UCSC Ensembl
chr11:58907274..58949973hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3842700
hg1942700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1198n223
Supporting Variantsnssv18184783
Samples
Known GenesDTX4, FAM111A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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