A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475321



Internal ID21132874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84287801..84291900hg38UCSC Ensembl
chr11:83998844..84002943hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994443
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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