A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049781



Internal ID19139000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81715095..81809042hg38UCSC Ensembl
Innerchr15:82007436..82101383hg19UCSC Ensembl
Innerchr15:79794491..79888438hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3893948
hg1993948
hg1893948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n100
Supporting Variantsnssv3554614
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)nsv1049781
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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