A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039545



Internal ID19128764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435409..34570510hg38UCSC Ensembl
Innerchr15:34727610..34862711hg19UCSC Ensembl
Innerchr15:32514902..32650003hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135102
hg19135102
hg18135102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3551607, nssv3551605, nssv3551602, nssv3551592, nssv3551597, nssv3551601, nssv3551608, nssv3551594, nssv3716629, nssv3551596, nssv3551603, nssv3551600, nssv3551591, nssv3551598, nssv3551604, nssv3551606, nssv3551593, nssv3551595, nssv3551599
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039545
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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