A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020745



Internal ID22082376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27489655..27609204hg38UCSC Ensembl
Outerchr5:27486816..27617078hg38UCSC Ensembl
Innerchr5:27489762..27609311hg19UCSC Ensembl
Outerchr5:27486923..27617185hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38130263
hg19130263
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156325
Supporting Variants
Samples
Known GenesLINC01021
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020745
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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