A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3540849



Internal ID18839130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..21096875hg38UCSC Ensembl
Innerchr15:20611357..21302204hg19UCSC Ensembl
Innerchr15:18871371..19566863hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38690772
hg19690848
hg18695493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036988
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3540849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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