A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037852



Internal ID19127071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22023848hg38UCSC Ensembl
Innerchr15:20262224..22311799hg19UCSC Ensembl
Innerchr15:18522238..19813163hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381966878
hg192049576
hg181290926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3538403, nssv3538405, nssv3538404, nssv3538406, nssv3715873
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)nsv1037852
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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