A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554627



Internal ID18506222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84129554..84388494hg38UCSC Ensembl
Innerchr15:84798306..84943192hg19UCSC Ensembl
Innerchr15:82589310..82734196hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38258941
hg19144887
hg18144887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041879
Supporting Variants
Samples
Known GenesDNM1P41, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554627
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