A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3553596



Internal ID18851877
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 StatusS
Merged Variantsnsv1043074
Supporting Variants
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)nssv3553596
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer