A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043958



Internal ID19133177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20674502hg38UCSC Ensembl
Innerchr15:20585976..20879831hg19UCSC Ensembl
Innerchr15:18845990..19139845hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38293780
hg19293856
hg18293856
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2231n100
Supporting Variantsnssv3537251, nssv3714636, nssv3537252, nssv3537253
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043958
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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