A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469220



Internal ID21126773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61271801..61273200hg38UCSC Ensembl
chr11:61039273..61040672hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190524
Samples
Known GenesVWCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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