A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536263



Internal ID18834544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..22283866hg38UCSC Ensembl
Innerchr15:20541968..22571817hg19UCSC Ensembl
Innerchr15:18801982..20073181hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381947152
hg192029850
hg181271200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052028
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536263
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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