A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049197



Internal ID19138416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19938398hg38UCSC Ensembl
Innerchr15:20016316..20143651hg19UCSC Ensembl
Innerchr15:18276329..18403665hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38127336
hg19127336
hg18127337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n100
Supporting Variantsnssv3714549, nssv3714551, nssv3714550, nssv3534406, nssv3714548
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)nsv1049197
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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