A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571640



Internal ID16012363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21654995..21728953hg38UCSC Ensembl
Innerchr16:21666316..21740274hg19UCSC Ensembl
Innerchr16:21573817..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3873959
hg1973959
hg1873959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149632
SamplesHGDP00700
Known GenesMETTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571640
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