A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456732



Internal ID21114285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132794782..132838069hg38UCSC Ensembl
chr11:132664677..132707964hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3843288
hg1943288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988061
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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