A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312383



Internal ID22274580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18341502..18343986hg38UCSC Ensembl
chr4:18343125..18345609hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3248678
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312383
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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