A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156416



Internal ID22086817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178682974..178686162hg38UCSC Ensembl
Outerchr5:178680821..178691854hg38UCSC Ensembl
Innerchr5:178109975..178113163hg19UCSC Ensembl
Outerchr5:178107822..178118855hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3811034
hg1911034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018087, nssv4018071, nssv4018089, nssv4018099, nssv4018073, nssv4018084, nssv4018063, nssv4018078, nssv4018100, nssv4018090, nssv4018062, nssv4018080, nssv4018047, nssv4018049, nssv4018069, nssv4018051, nssv4018052, nssv4018056, nssv4018095, nssv4018072, nssv4018070, nssv4018057, nssv4018081, nssv4018088, nssv4018059, nssv4018104, nssv4018093, nssv4018098, nssv4018096, nssv4018065, nssv4018085, nssv4018064, nssv4018101, nssv4018054, nssv4018076, nssv4018102, nssv4018074, nssv4018055, nssv4018103, nssv4018067, nssv4018094, nssv4018061, nssv4018083, nssv4018075, nssv4018066, nssv4018050, nssv4018097, nssv4018060, nssv4018092, nssv4018068, nssv4018077, nssv4018082, nssv4018079, nssv4018091, nssv4018086, nssv4018058, nssv4018105, nssv4018053, nssv4018048
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156416
Frequency
Sample Size131
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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