A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050109



Internal ID18792640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34585552hg38UCSC Ensembl
Innerchr15:34695310..34877753hg19UCSC Ensembl
Innerchr15:32482602..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38182444
hg19182444
hg18182444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2554n100
Supporting Variantsnssv3548846, nssv3548845, nssv3548847
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)nsv1050109
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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