A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047384



Internal ID18789915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89498372..89571078hg38UCSC Ensembl
Innerchr15:90041603..90114309hg19UCSC Ensembl
Innerchr15:87842607..87915313hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3872707
hg1972707
hg1872707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718188
Samples
Known GenesLINC00928
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047384
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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