A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475159



Internal ID21132712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131995773..132141588hg38UCSC Ensembl
chr11:131865667..132011482hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38145816
hg19145816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192370
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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