A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046027



Internal ID19135246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38834534..38867666hg38UCSC Ensembl
Innerchr15:39126735..39159867hg19UCSC Ensembl
Innerchr15:36914027..36947159hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3833133
hg1933133
hg1833133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2577n100
Supporting Variantsnssv3552242
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)nsv1046027
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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