A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043007



Internal ID19132226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20996195hg38UCSC Ensembl
Innerchr15:20262224..21201524hg19UCSC Ensembl
Innerchr15:18522238..19466183hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38939225
hg19939301
hg18943946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2182n100
Supporting Variantsnssv3538388, nssv3538387, nssv3538386, nssv3715862
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)nsv1043007
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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