A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4440n54



Internal ID22772335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31674564..32240135hg38UCSC Ensembl
chr15:31966767..32532336hg19UCSC Ensembl
chr15:29754059..30319628hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38565572
hg19565570
hg18565570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568828, nsv568831, nsv568841, nsv568830, nsv568839, nsv568842, nsv568826, nsv568838, nsv568827, nsv568837, nsv568843, nsv568845, nsv568844, nsv568833, nsv568836, nsv568846, nsv568835, nsv568829, nsv568832
Samples1780862263_A, NINDS_35, NINDS_182, HGDP00570, NINDS_31, HGDP00148, HGDP00976, HGDP00474, HGDP00594, HGDP00564
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4440n54
Frequency
Sample Size17421
Observed Gain40
Observed Loss0
Observed Complex0
Frequencyn/a


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