A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv996n145



Internal ID22814012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151386886..151419218hg38UCSC Ensembl
chr5:150766447..150798779hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3832333
hg1932333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113438, nsv3113775
Samplessample84, sample282, sample150
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv996n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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