A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042726



Internal ID18785257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435409..34565797hg38UCSC Ensembl
Innerchr15:34727610..34857998hg19UCSC Ensembl
Innerchr15:32514902..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38130389
hg19130389
hg18130389
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3551579, nssv3551560, nssv3551552, nssv3716626, nssv3716619, nssv3551565, nssv3551574, nssv3716623, nssv3551570, nssv3551586, nssv3716625, nssv3551564, nssv3551585, nssv3551576, nssv3551582, nssv3551588, nssv3551587, nssv3716622, nssv3551548, nssv3716628, nssv3551550, nssv3716621, nssv3551563, nssv3551561, nssv3551558, nssv3551545, nssv3716627, nssv3551569, nssv3551568, nssv3551571, nssv3551556, nssv3716624, nssv3551559, nssv3551575, nssv3716620, nssv3551555, nssv3551578, nssv3551573, nssv3551584, nssv3551577, nssv3551549, nssv3551566, nssv3551580, nssv3551562, nssv3551554, nssv3551583, nssv3551567, nssv3551551, nssv3551572, nssv3551553, nssv3551589, nssv3551546, nssv3551547, nssv3551557, nssv3551581
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)nsv1042726
Frequency
Sample Size29084
Observed Gain1
Observed Loss54
Observed Complex0
Frequencyn/a


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