A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906103



Internal ID22681298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50798243..50798553hg38UCSC Ensembl
chr6:50765956..50766266hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906103
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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