A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471837



Internal ID21129390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119100401..119103900hg38UCSC Ensembl
chr11:118971111..118974610hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986651
Samples
Known GenesDPAGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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