A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043642



Internal ID19132861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34427582..34565797hg38UCSC Ensembl
Innerchr15:34719783..34857998hg19UCSC Ensembl
Innerchr15:32507075..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38138216
hg19138216
hg18138216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3549006, nssv3549017, nssv3549007, nssv3549003, nssv3721832, nssv3549008, nssv3549011, nssv3549016, nssv3549013, nssv3549010, nssv3549015, nssv3549005, nssv3721833, nssv3549004, nssv3549014, nssv3549012, nssv3549018, nssv3549009
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)nsv1043642
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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