A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606168



Internal ID16393577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9694694..10786567hg38UCSC Ensembl
Innerchr7:9734323..10826194hg19UCSC Ensembl
Innerchr7:9700848..10792719hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381091874
hg191091872
hg181091872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079124
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606168
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