A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457051



Internal ID21114604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61841155..61843762hg38UCSC Ensembl
chr11:61608627..61611234hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195368
Samples
Known GenesFADS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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