A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2539n100



Internal ID22788626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32147032..32285928hg38UCSC Ensembl
chr15:32439233..32578129hg19UCSC Ensembl
chr15:30226525..30365421hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38138897
hg19138897
hg18138897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038072, nsv1041765, nsv1045626, nsv1042163, nsv1043782, nsv1042068
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2539n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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