A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156330



Internal ID22084806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38144944..38148786hg38UCSC Ensembl
Outerchr5:38144390..38149898hg38UCSC Ensembl
Innerchr5:38145046..38148888hg19UCSC Ensembl
Outerchr5:38144492..38150000hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg385509
hg195509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020794, nssv4020798, nssv4020780, nssv4020775, nssv4020800, nssv4020760, nssv4020765, nssv4020772, nssv4020793, nssv4020771, nssv4020763, nssv4020782, nssv4020784, nssv4020764, nssv4020802, nssv4020776, nssv4020781, nssv4020797, nssv4020767, nssv4020778, nssv4020787, nssv4020785, nssv4020774, nssv4020795, nssv4020766, nssv4020799, nssv4020773, nssv4020759, nssv4020777, nssv4020786, nssv4020756, nssv4020770, nssv4020758, nssv4020783, nssv4020791, nssv4020762, nssv4020796, nssv4020761, nssv4020754, nssv4020789, nssv4020769, nssv4020792, nssv4020788, nssv4020755
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156330
Frequency
Sample Size131
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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