A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714675



Internal ID19012956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22283155hg38UCSC Ensembl
Innerchr15:20585976..22571106hg19UCSC Ensembl
Innerchr15:18845990..20072470hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381902433
hg191985131
hg181226481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047580
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714675
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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