A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572537



Internal ID16013260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47377292..47565591hg38UCSC Ensembl
Innerchr16:47411203..47599502hg19UCSC Ensembl
Innerchr16:45968704..46157003hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38188300
hg19188300
hg18188300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856649
Samples
Known GenesITFG1, PHKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572537
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