A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605759



Internal ID16393168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1249643..1281040hg38UCSC Ensembl
Innerchr7:1289279..1320676hg19UCSC Ensembl
Innerchr7:1255805..1287202hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831398
hg1931398
hg1831398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11124n54
Supporting Variantsnssv1078108
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605759
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