A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047620



Internal ID19136839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..21096875hg38UCSC Ensembl
Innerchr15:20590015..21302204hg19UCSC Ensembl
Innerchr15:18850029..19566863hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38712114
hg19712190
hg18716835
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2246n100
Supporting Variantsnssv3539571, nssv3714775, nssv3539573, nssv3714776, nssv3539574, nssv3539572, nssv3539570
Samples
Known GenesCT60, 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)nsv1047620
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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