A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738678



Internal ID20514649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2512293..2512427hg38UCSC Ensembl
chr5:2512407..2512541hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738678
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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