A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037441



Internal ID19126660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22196402hg38UCSC Ensembl
Innerchr15:20564575..22484353hg19UCSC Ensembl
Innerchr15:18824589..19985717hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381837081
hg191919779
hg181161129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3537603
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)nsv1037441
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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