A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045603



Internal ID19134822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20670504hg38UCSC Ensembl
Innerchr15:20569939..20875833hg19UCSC Ensembl
Innerchr15:18829953..19135847hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38305819
hg19305895
hg18305895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2244n100
Supporting Variantsnssv3537651
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)nsv1045603
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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