A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039257



Internal ID19128476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20305889..22023848hg38UCSC Ensembl
Innerchr15:20511142..22311799hg19UCSC Ensembl
Innerchr15:18771156..19813163hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381717960
hg191800658
hg181042008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3536106
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1039257
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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