A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047941



Internal ID18790472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28110984..28168961hg38UCSC Ensembl
Innerchr15:28356130..28414107hg19UCSC Ensembl
Innerchr15:26029725..26087702hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3857978
hg1957978
hg1857978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545664
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)nsv1047941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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