A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043074



Internal ID19132293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57351455..57486837hg38UCSC Ensembl
Innerchr15:57643653..57779035hg19UCSC Ensembl
Innerchr15:55430945..55566327hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38135383
hg19135383
hg18135383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553594, nssv3553597, nssv3717939, nssv3717940, nssv3717941, nssv3553596, nssv3553595, nssv3553593
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)nsv1043074
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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