A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050266



Internal ID19139485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20336715hg38UCSC Ensembl
Innerchr15:20284054..20541968hg19UCSC Ensembl
Innerchr15:18544068..18801982hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38257915
hg19257915
hg18257915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3539958
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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