A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046874



Internal ID18789405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30715930..31002451hg38UCSC Ensembl
Innerchr15:31008133..31294654hg19UCSC Ensembl
Innerchr15:28795425..29081946hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38286522
hg19286522
hg18286522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3721586
Samples
Known GenesFAN1, HERC2P10, LOC100288637, MIR7976, MTMR10, TRPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046874
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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