A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040146



Internal ID18782677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20898495..21992514hg38UCSC Ensembl
Innerchr15:21103824..22280465hg19UCSC Ensembl
Innerchr15:19368467..19781829hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381094020
hg191176642
hg18413363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541381
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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