A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054023



Internal ID19143242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20396289..21078935hg38UCSC Ensembl
Innerchr15:20601542..21284264hg19UCSC Ensembl
Innerchr15:18861556..19548923hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38682647
hg19682723
hg18687368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3539668, nssv3714793, nssv3539669
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1054023
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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