A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890252



Internal ID22665278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25586064..25586146hg38UCSC Ensembl
chr6:25586292..25586374hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432444
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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