A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906939



Internal ID22682143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91651177..91651618hg38UCSC Ensembl
chr5:90946994..90947435hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906939
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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