A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045942



Internal ID19135161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34538175hg38UCSC Ensembl
Innerchr15:34695310..34830376hg19UCSC Ensembl
Innerchr15:32482602..32617668hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135067
hg19135067
hg18135067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3548691, nssv3548694, nssv3548696, nssv3548690, nssv3548689, nssv3548695, nssv3548692, nssv3548693
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)nsv1045942
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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