A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2533n100



Internal ID19012901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30628409..30818328hg38UCSC Ensembl
chr15:30920612..31110531hg19UCSC Ensembl
chr15:28707904..28897823hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38189920
hg19189920
hg18189920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046832, nsv1040040, nsv1039621, nsv1039677, nsv1035952
Samples
Known GenesARHGAP11B, HERC2P10, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2533n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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