A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154889



Internal ID22085394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31958485..31964286hg38UCSC Ensembl
Outerchr13:31957984..31965910hg38UCSC Ensembl
Innerchr13:32532622..32538423hg19UCSC Ensembl
Outerchr13:32532121..32540047hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg387927
hg197927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv68n97
Supporting Variantsnssv4006978, nssv4006993, nssv4006990, nssv4010472, nssv4006980, nssv4006984, nssv4006994, nssv4006996, nssv4006977, nssv4010471, nssv4006979, nssv4010469, nssv4006981, nssv4006985, nssv4006987, nssv4006989, nssv4006976, nssv4006995, nssv4006991, nssv4006983, nssv4010468, nssv4006982, nssv4006992, nssv4006986, nssv4006988, nssv4010470
Samples
Known GenesEEF1DP3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154889
Frequency
Sample Size131
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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