A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546676



Internal ID18498271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30261691..30608663hg38UCSC Ensembl
Innerchr15:30553894..30900866hg19UCSC Ensembl
Innerchr15:28341186..28688158hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38346973
hg19346973
hg18346973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049226
Supporting Variants
Samples
Known GenesCHRFAM7A, 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)nssv3546676
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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