A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607789



Internal ID16395198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90537591..90585619hg38UCSC Ensembl
Innerchr7:90166905..90214933hg19UCSC Ensembl
Innerchr7:90004841..90052869hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3848029
hg1948029
hg1848029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11498n54
Supporting Variantsnssv1155363
SamplesHGDP00776
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607789
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