A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041378



Internal ID19130597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22199979hg38UCSC Ensembl
Innerchr15:20262224..22487930hg19UCSC Ensembl
Innerchr15:18522238..19989294hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382143009
hg192225707
hg181467057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3538426
Samples
Known GenesCHEK2P2, CT60, 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)nsv1041378
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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