A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052479



Internal ID19141698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34538731hg38UCSC Ensembl
Innerchr15:34722790..34830932hg19UCSC Ensembl
Innerchr15:32510082..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38108143
hg19108143
hg18108143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3549657, nssv3549654, nssv3549653, nssv3549660, nssv3549662, nssv3549659, nssv3721921, nssv3549656, nssv3549651, nssv3549649, nssv3549658, nssv3549652, nssv3549661, nssv3549655, nssv3549650
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)nsv1052479
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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