A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049364



Internal ID18791895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30608663hg38UCSC Ensembl
Innerchr15:30505066..30900866hg19UCSC Ensembl
Innerchr15:28292358..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38395801
hg19395801
hg18395801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2504n100
Supporting Variantsnssv3546660
Samples
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8H, LOC101059918, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049364
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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