A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045264



Internal ID19134483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54689340..54811579hg38UCSC Ensembl
Innerchr15:54981538..55103777hg19UCSC Ensembl
Innerchr15:52768830..52891069hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38122240
hg19122240
hg18122240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552439, nssv3552438
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045264
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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