A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553968



Internal ID16341377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372799..31375881hg38UCSC Ensembl
Innerchr11:31394346..31397428hg19UCSC Ensembl
Innerchr11:31350922..31354004hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383083
hg193083
hg183083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n54
Supporting Variantsnssv770976, nssv770987, nssv771000, nssv770981, nssv770995, nssv770999, nssv770979, nssv771008, nssv771002, nssv770977, nssv770993, nssv770978, nssv770972, nssv770996, nssv771004, nssv771010, nssv771009, nssv770971, nssv770992, nssv770974, nssv771006, nssv770975, nssv771011, nssv771007, nssv771005, nssv770988, nssv770980, nssv770970, nssv771003, nssv770990, nssv770986, nssv770991, nssv770998, nssv771001, nssv770983, nssv770984, nssv770985, nssv770994, nssv770982, nssv770973, nssv770997, nssv770989
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553968
Frequency
Sample Size17421
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer