A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14319401



Internal ID22323899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5810256..5810556hg38UCSC Ensembl
chr5:5810369..5810669hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557617
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14319401
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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