A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045577



Internal ID18788108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22472558hg38UCSC Ensembl
Innerchr15:20564575..22751233hg19UCSC Ensembl
Innerchr15:18824589..20302597hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382113237
hg192186659
hg181478009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n100
Supporting Variantsnssv3537625
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)nsv1045577
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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