A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041428



Internal ID19130647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..22046199hg38UCSC Ensembl
Innerchr15:20203949..22334150hg19UCSC Ensembl
Innerchr15:18463963..19835514hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382047504
hg192130202
hg181371552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3534532, nssv3534531, nssv3534530
Samples
Known GenesCHEK2P2, CT60, 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)nsv1041428
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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