A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046861



Internal ID19136080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22151555hg38UCSC Ensembl
Innerchr15:20564575..22439506hg19UCSC Ensembl
Innerchr15:18824589..19940870hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381792234
hg191874932
hg181116282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3537598
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)nsv1046861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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