A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892800



Internal ID22667855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138553442..138553588hg38UCSC Ensembl
chr5:137889131..137889277hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892800
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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