A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360420



Internal ID22269168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17436310..17448427hg38UCSC Ensembl
chr12:17589244..17601361hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3812118
hg1912118
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3245474
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360420
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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