A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044116



Internal ID19133335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22472558hg38UCSC Ensembl
Innerchr15:20284054..22751244hg19UCSC Ensembl
Innerchr15:18544068..20302608hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382393758
hg192467191
hg181758541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2183n100
Supporting Variantsnssv3537905
Samples
Known GenesCHEK2P2, CT60, 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)nsv1044116
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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