A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035244



Internal ID19124463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20401433..22046199hg38UCSC Ensembl
Innerchr15:20606686..22334150hg19UCSC Ensembl
Innerchr15:18866700..19835514hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381644767
hg191727465
hg18968815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3540830, nssv3540831
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)nsv1035244
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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