A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045994



Internal ID19135213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81715095..81796857hg38UCSC Ensembl
Innerchr15:82007436..82089198hg19UCSC Ensembl
Innerchr15:79794491..79876253hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3881763
hg1981763
hg1881763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n100
Supporting Variantsnssv3554613
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)nsv1045994
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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