A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555289



Internal ID18506884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98933915..99479656hg38UCSC Ensembl
Innerchr15:99477144..100019861hg19UCSC Ensembl
Innerchr15:97294667..97837384hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38545742
hg19542718
hg18542718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055008
Supporting Variants
Samples
Known GenesHSP90B2P, IGF1R, LRRC28, PGPEP1L, SYNM, TTC23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555289
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