A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054402



Internal ID18796933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28110984..28199610hg38UCSC Ensembl
Innerchr15:28356130..28444756hg19UCSC Ensembl
Innerchr15:26029725..26118351hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3888627
hg1988627
hg1888627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2490n100
Supporting Variantsnssv3545667
Samples
Known GenesHERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054402
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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