A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5836n100



Internal ID22791923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176038674..176241562hg38UCSC Ensembl
chr5:175465677..175668565hg19UCSC Ensembl
chr5:175398283..175601171hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38202889
hg19202889
hg18202889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028117, nsv1027995
Samples
Known GenesFAM153B, LOC100507387, LOC100996385, LOC643201, SIMC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5836n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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