A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721481



Internal ID18673076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30488448hg38UCSC Ensembl
Innerchr15:30386399..30780651hg19UCSC Ensembl
Innerchr15:28173691..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38394253
hg19394253
hg18394253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047974
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721481
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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