A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038344



Internal ID19127563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..20688370hg38UCSC Ensembl
Innerchr15:20541968..20893699hg19UCSC Ensembl
Innerchr15:18801982..19153713hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38351656
hg19351732
hg18351732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2233n100
Supporting Variantsnssv3536251
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038344
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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