A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2541n100



Internal ID22788628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32166460..32387416hg38UCSC Ensembl
chr15:32458661..32679617hg19UCSC Ensembl
chr15:30245953..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38220957
hg19220957
hg18220957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053539, nsv1041649, nsv1042737, nsv1053605, nsv1044976, nsv1040905, nsv1041793, nsv1039606
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)dgv2541n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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