A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547803



Internal ID18846084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32217691..32387416hg38UCSC Ensembl
Innerchr15:32509892..32679617hg19UCSC Ensembl
Innerchr15:30297184..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38169726
hg19169726
hg18169726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041793
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547803
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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