A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981353



Internal ID12626539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31716805..32113007hg38UCSC Ensembl
Innerchr15:32009008..32405208hg19UCSC Ensembl
Innerchr15:29796300..30192500hg18UCSC Ensembl
Innerchr15:29796300..30192500hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38396203
hg19396201
hg18396201
hg17396201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751531
Supporting Variants
SamplesBEC_394
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981353
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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