A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573424



Internal ID16014147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84182086..84215151hg38UCSC Ensembl
Innerchr16:84215692..84248757hg19UCSC Ensembl
Innerchr16:82773193..82806258hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833066
hg1933066
hg1833066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149333
SamplesNINDS_6
Known GenesADAD2, TAF1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573424
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