A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14323569



Internal ID22227273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146064705..146069996hg38UCSC Ensembl
chr5:145444268..145449559hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385292
hg195292
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244703
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14323569
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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