A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571022



Internal ID16358431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:718334..728820hg38UCSC Ensembl
Innerchr16:768334..778820hg19UCSC Ensembl
Innerchr16:708335..718821hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810487
hg1910487
hg1810487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851747
Samples
Known GenesCCDC78, FAM173A, HAGHL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571022
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