A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041708



Internal ID18784239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30152061..30487481hg38UCSC Ensembl
Innerchr15:30444264..30779684hg19UCSC Ensembl
Innerchr15:28231556..28566976hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38335421
hg19335421
hg18335421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3546487
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041708
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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