A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037267



Internal ID18779798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..22472558hg38UCSC Ensembl
Innerchr15:20541968..22756014hg19UCSC Ensembl
Innerchr15:18801982..20307378hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382135844
hg192214047
hg181505397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n100
Supporting Variantsnssv3536292
Samples
Known GenesCT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, 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)nsv1037267
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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