A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902947



Internal ID22678109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155085401..155091433hg38UCSC Ensembl
chr5:154464961..154470993hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg386033
hg196033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902947
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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