A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474900



Internal ID21132453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46098438..46098927hg38UCSC Ensembl
chr11:46119989..46120478hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991752
Samples
Known GenesPHF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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