A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896109



Internal ID22671198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138143607..138143672hg38UCSC Ensembl
chr5:137479296..137479361hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413481
Samples
Known GenesBRD8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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