A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047522



Internal ID19136741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430431..34538731hg38UCSC Ensembl
Innerchr15:34722632..34830932hg19UCSC Ensembl
Innerchr15:32509924..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38108301
hg19108301
hg18108301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3549537, nssv3549525, nssv3549542, nssv3549530, nssv3549547, nssv3549529, nssv3549538, nssv3549546, nssv3549544, nssv3549545, nssv3549540, nssv3721878, nssv3549528, nssv3549523, nssv3549536, nssv3549534, nssv3549526, nssv3721879, nssv3721877, nssv3549532, nssv3549548, nssv3549521, nssv3549539, nssv3549531, nssv3549527, nssv3549543, nssv3721876, nssv3549524, nssv3721875, nssv3549541, nssv3549533, nssv3549522, nssv3549535
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)nsv1047522
Frequency
Sample Size11257
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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