A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14364834



Internal ID22118898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:88339326..88345232hg38UCSC Ensembl
chr12:88733103..88739009hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg385907
hg195907
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3241080
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14364834
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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