A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459142



Internal ID21116695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34619373..34767757hg38UCSC Ensembl
chr11:34640920..34789304hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38148385
hg19148385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179771
Samples
Known GenesEHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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