A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460088



Internal ID21117641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127777201..127782400hg38UCSC Ensembl
chr11:127647096..127652295hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1334n223
Supporting Variantsnssv18180042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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