A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041484



Internal ID18784015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28110984..28195141hg38UCSC Ensembl
Innerchr15:28356130..28440287hg19UCSC Ensembl
Innerchr15:26029725..26113882hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3884158
hg1984158
hg1884158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2490n100
Supporting Variantsnssv3545666
Samples
Known GenesHERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041484
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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