A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045506



Internal ID19134725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352069..57486837hg38UCSC Ensembl
Innerchr15:57644267..57779035hg19UCSC Ensembl
Innerchr15:55431559..55566327hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38134769
hg19134769
hg18134769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553602, nssv3553604, nssv3553603, nssv3553601
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)nsv1045506
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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