A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473690



Internal ID21131243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131934501..132124500hg38UCSC Ensembl
chr11:131804395..131994394hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38190000
hg19190000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988542
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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