A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051464



Internal ID19140683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438889..34538731hg38UCSC Ensembl
Innerchr15:34731090..34830932hg19UCSC Ensembl
Innerchr15:32518382..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3899843
hg1999843
hg1899843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3551669, nssv3551671, nssv3551667, nssv3551668, nssv3716637, nssv3551672, nssv3716638, nssv3551673, nssv3716636, nssv3551666, nssv3551670, nssv3551674
Samples
Known GenesGOLGA8B, 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)nsv1051464
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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