A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607771



Internal ID16395180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89892613..89901665hg38UCSC Ensembl
Innerchr7:89521927..89530979hg19UCSC Ensembl
Innerchr7:89359863..89368915hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg389053
hg199053
hg189053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11495n54
Supporting Variantsnssv1089564
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607771
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