A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052172



Internal ID19141391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101491141..101612385hg38UCSC Ensembl
Innerchr15:102031344..102152588hg19UCSC Ensembl
Innerchr15:99848867..99970111hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38121245
hg19121245
hg18121245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2678n100
Supporting Variantsnssv3555360, nssv3718224, nssv3718225
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)nsv1052172
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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