A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055092



Internal ID19144311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..21018342hg38UCSC Ensembl
Innerchr15:20585976..21223671hg19UCSC Ensembl
Innerchr15:18845990..19488330hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38637620
hg19637696
hg18642341
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2246n100
Supporting Variantsnssv3537286, nssv3537284, nssv3537285, nssv3537287, nssv3537283
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)nsv1055092
Frequency
Sample Size11257
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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