A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14306643



Internal ID22224912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62333958..62335794hg38UCSC Ensembl
chr3:62319633..62321469hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3237483
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14306643
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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