A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045360



Internal ID18787891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34408470..34563605hg38UCSC Ensembl
Innerchr15:34700671..34855806hg19UCSC Ensembl
Innerchr15:32487963..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38155136
hg19155136
hg18155136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2554n100
Supporting Variantsnssv3721753, nssv3548885, nssv3721754, nssv3721752, nssv3548886, nssv3548884, nssv3721751
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)nsv1045360
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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