A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036530



Internal ID19125749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..22199184hg38UCSC Ensembl
Innerchr15:20203949..22487135hg19UCSC Ensembl
Innerchr15:18463963..19988499hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382200489
hg192283187
hg181524537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3534546
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, 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)nsv1036530
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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