A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041232



Internal ID19130451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34565797hg38UCSC Ensembl
Innerchr15:34722790..34857998hg19UCSC Ensembl
Innerchr15:32510082..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135209
hg19135209
hg18135209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3549679, nssv3549682, nssv3549680, nssv3549674, nssv3721924, nssv3549671, nssv3549677, nssv3549683, nssv3721926, nssv3549678, nssv3549672, nssv3549675, nssv3721925, nssv3549673, nssv3549676, nssv3549681, nssv3549684
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)nsv1041232
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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