A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042028



Internal ID19131247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27666188..27682648hg38UCSC Ensembl
Innerchr15:27911334..27927794hg19UCSC Ensembl
Innerchr15:25584929..25601389hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816461
hg1916461
hg1816461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2487n100
Supporting Variantsnssv3545646
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042028
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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