A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903315



Internal ID22678481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87869793..87869863hg38UCSC Ensembl
chr5:87165610..87165680hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903315
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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