A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036602



Internal ID19125821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..22046199hg38UCSC Ensembl
Innerchr15:20216943..22334150hg19UCSC Ensembl
Innerchr15:18476957..19835514hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382034510
hg192117208
hg181358558
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n100
Supporting Variantsnssv3537009, nssv3537008, nssv3537006, nssv3537010, nssv3537007
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)nsv1036602
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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