A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606226



Internal ID16393635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12389177..12465747hg38UCSC Ensembl
Innerchr7:12428803..12505373hg19UCSC Ensembl
Innerchr7:12395328..12471898hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3876571
hg1976571
hg1876571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11207n54
Supporting Variantsnssv1079183
Samples
Known GenesVWDE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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