A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447556



Internal ID21105109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12053060..12061149hg38UCSC Ensembl
chr11:12074607..12082696hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg388090
hg198090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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