A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474131



Internal ID21131684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74350901..74357600hg38UCSC Ensembl
chr11:74061946..74068645hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196932
Samples
Known GenesPGM2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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