A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156378



Internal ID22086779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370746..115385388hg38UCSC Ensembl
Outerchr5:115369510..115387269hg38UCSC Ensembl
Innerchr5:114706443..114721085hg19UCSC Ensembl
Outerchr5:114705207..114722966hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3817760
hg1917760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv233n97
Supporting Variantsnssv4018992, nssv4018993, nssv4018994
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156378
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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