A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038940



Internal ID19128159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..22209017hg38UCSC Ensembl
Innerchr15:20569939..22496968hg19UCSC Ensembl
Innerchr15:18829953..19998332hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381844332
hg191927030
hg181168380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3535795
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)nsv1038940
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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