A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896859



Internal ID22671955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40262961..40264640hg38UCSC Ensembl
chr5:40263063..40264742hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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