A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902732



Internal ID22677893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133936366..133936645hg38UCSC Ensembl
chr5:133272057..133272336hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902732
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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