A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048967



Internal ID18791498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34447659..34565797hg38UCSC Ensembl
Innerchr15:34739860..34857998hg19UCSC Ensembl
Innerchr15:32527152..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38118139
hg19118139
hg18118139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2570n100
Supporting Variantsnssv3552103, nssv3552105, nssv3552104
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)nsv1048967
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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