A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547649



Internal ID18845930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30654103..30818328hg38UCSC Ensembl
Innerchr15:30946306..31110531hg19UCSC Ensembl
Innerchr15:28733598..28897823hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38164226
hg19164226
hg18164226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053014
Supporting Variants
Samples
Known GenesHERC2P10, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547649
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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