A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554644



Internal ID18506239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84153209..84546378hg38UCSC Ensembl
Innerchr15:84821961..85089609hg19UCSC Ensembl
Innerchr15:82612965..82890613hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38393170
hg19267649
hg18277649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054646
Supporting Variants
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554644
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