A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605593



Internal ID16393002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..113319hg38UCSC Ensembl
Innerchr7:45653..113319hg19UCSC Ensembl
Innerchr7:140736..208402hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3867667
hg1967667
hg1867667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155835, nssv1155837, nssv1155838, nssv1155836
SamplesHGDP01093, HGDP01091, HGDP00538, HGDP01036
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605593
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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