A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475229



Internal ID21132782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67484151..67485980hg38UCSC Ensembl
chr11:67251622..67253451hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381830
hg191830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993492
Samples
Known GenesAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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