A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044722



Internal ID19133941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101491141..101611170hg38UCSC Ensembl
Innerchr15:102031344..102151373hg19UCSC Ensembl
Innerchr15:99848867..99968896hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38120030
hg19120030
hg18120030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2678n100
Supporting Variantsnssv3555359, nssv3555357, nssv3555358, nssv3555356
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)nsv1044722
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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