A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572759



Internal ID16013482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57972385..58040306hg38UCSC Ensembl
Innerchr16:58006289..58074210hg19UCSC Ensembl
Innerchr16:56563790..56631711hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3867922
hg1967922
hg1867922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858144
Samples
Known GenesMMP15, TEPP, USB1, ZNF319
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572759
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