A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893782



Internal ID22668847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176430386..176430588hg38UCSC Ensembl
chr5:175857387..175857589hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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