A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052129



Internal ID19141348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94484728..94545815hg38UCSC Ensembl
Innerchr15:95027957..95089044hg19UCSC Ensembl
Innerchr15:92828961..92890048hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3861088
hg1961088
hg1861088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555281
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)nsv1052129
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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