A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039371



Internal ID19128590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20992019hg38UCSC Ensembl
Innerchr15:20262224..21197348hg19UCSC Ensembl
Innerchr15:18522238..19462007hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38935049
hg19935125
hg18939770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2182n100
Supporting Variantsnssv3715861
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, 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)nsv1039371
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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