A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572617



Internal ID16013340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53114148..53287822hg38UCSC Ensembl
Innerchr16:53148060..53321734hg19UCSC Ensembl
Innerchr16:51705561..51879235hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38173675
hg19173675
hg18173675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857462
Samples
Known GenesCHD9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572617
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