A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041096



Internal ID19130315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19950373hg38UCSC Ensembl
Innerchr15:20016316..20155626hg19UCSC Ensembl
Innerchr15:18276329..18415640hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38139311
hg19139311
hg18139312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n100
Supporting Variantsnssv3534417, nssv3715685, nssv3534416, nssv3534414, nssv3534412, nssv3715686, nssv3534413, nssv3534415, nssv3715687, nssv3715688
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)nsv1041096
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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