A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888270



Internal ID22663273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42108284..42108394hg38UCSC Ensembl
chr5:42108386..42108496hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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