A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895377



Internal ID22670459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139547653..139553916hg38UCSC Ensembl
chr5:138927238..138933501hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg386264
hg196264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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