A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894547



Internal ID22669620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62278948..62280678hg38UCSC Ensembl
chr5:61574775..61576505hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381731
hg191731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894547
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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