A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047777



Internal ID19136996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20929146hg38UCSC Ensembl
Innerchr15:20585976..21134475hg19UCSC Ensembl
Innerchr15:18845990..19399134hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38548424
hg19548500
hg18553145
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2246n100
Supporting Variantsnssv3537266, nssv3537265, nssv3714649
Samples
Known GenesCXADRP2, 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)nsv1047777
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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