A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475205



Internal ID21132758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131868563..131869156hg38UCSC Ensembl
chr11:131738457..131739050hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988536
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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