A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900910



Internal ID22676057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176806330..176810987hg38UCSC Ensembl
chr5:176233331..176237988hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg384658
hg194658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424195
Samples
Known GenesUNC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900910
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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