A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048242



Internal ID18790773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20942515..22095238hg38UCSC Ensembl
Innerchr15:21147844..22383189hg19UCSC Ensembl
Innerchr15:19412503..19884553hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381152724
hg191235346
hg18472051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541488
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N4, 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)nsv1048242
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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