A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040066



Internal ID19129285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57354934..57489367hg38UCSC Ensembl
Innerchr15:57647132..57781565hg19UCSC Ensembl
Innerchr15:55434424..55568857hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38134434
hg19134434
hg18134434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553606
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040066
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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