A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456068



Internal ID21113621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61663001..61665200hg38UCSC Ensembl
chr11:61430473..61432672hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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