A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038861



Internal ID19128080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..22134397hg38UCSC Ensembl
Innerchr15:20590015..22422348hg19UCSC Ensembl
Innerchr15:18850029..19923712hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381749636
hg191832334
hg181073684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3714778
Samples
Known GenesCT60, 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)nsv1038861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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