A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2525n100



Internal ID20154141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30438488..30688830hg38UCSC Ensembl
chr15:30730691..30981033hg19UCSC Ensembl
chr15:28517983..28768325hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38250343
hg19250343
hg18250343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040737, nsv1038659, nsv1042578, nsv1042653, nsv1053813, nsv1035220, nsv1040287, nsv1038251, nsv1047175, nsv1040596, nsv1039160, nsv1045627
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2525n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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