A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718097



Internal ID18669692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81257750..81343926hg38UCSC Ensembl
Innerchr15:81550091..81636267hg19UCSC Ensembl
Innerchr15:79337146..79423322hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3886177
hg1986177
hg1886177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048788
Supporting Variants
Samples
Known GenesIL16, STARD5, TMC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718097
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