A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552411



Internal ID18850692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52870720..52895311hg38UCSC Ensembl
Innerchr15:53162917..53187508hg19UCSC Ensembl
Innerchr15:50950209..50974800hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3824592
hg1924592
hg1824592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043999
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)nssv3552411
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