A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607730



Internal ID16395139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87701107..87723256hg38UCSC Ensembl
Innerchr7:87330423..87352572hg19UCSC Ensembl
Innerchr7:87168359..87190508hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3822150
hg1922150
hg1822150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11489n54
Supporting Variantsnssv1089389
Samples
Known GenesABCB1, RUNDC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607730
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