A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041649



Internal ID19130868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32196661..32387416hg38UCSC Ensembl
Innerchr15:32488862..32679617hg19UCSC Ensembl
Innerchr15:30276154..30466909hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38190756
hg19190756
hg18190756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2541n100
Supporting Variantsnssv3547794
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)nsv1041649
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