A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552414



Internal ID18850695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52984196..53024313hg38UCSC Ensembl
Innerchr15:53276393..53316510hg19UCSC Ensembl
Innerchr15:51063685..51103802hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3840118
hg1940118
hg1840118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037269
Supporting Variants
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)nssv3552414
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