A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3248678



Internal ID22377049
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312383
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3248678
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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