A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055068



Internal ID18797599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..22133448hg38UCSC Ensembl
Innerchr15:20016316..22421399hg19UCSC Ensembl
Innerchr15:18276329..19922763hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382322386
hg192405084
hg181646435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n100
Supporting Variantsnssv3715693
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, 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)nsv1055068
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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