A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610794



Internal ID16398203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25113490..25129840hg38UCSC Ensembl
Innerchr8:24971005..24987355hg19UCSC Ensembl
Innerchr8:25026922..25043272hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3816351
hg1916351
hg1816351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12062n54
Supporting Variantsnssv1107520
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610794
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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