A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573051



Internal ID16360460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76616646..76765083hg38UCSC Ensembl
Innerchr16:76650543..76798980hg19UCSC Ensembl
Innerchr16:75208044..75356481hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38148438
hg19148438
hg18148438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv860371
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573051
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