A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554620



Internal ID18506215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82576576..82792509hg38UCSC Ensembl
Innerchr15:83245326..83461261hg19UCSC Ensembl
Innerchr15:81042381..81258315hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38215934
hg19215936
hg18215935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036950
Supporting Variants
Samples
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554620
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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