A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706340



Internal ID21228134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138143589..138143654hg38UCSC Ensembl
chr5:137479278..137479343hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810153
Supporting Variants
Samples
Known GenesBRD8
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706340
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.328125


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer