A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232659



Internal ID22372561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45348467..45354815hg38UCSC Ensembl
chr1:45814139..45820487hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg386349
hg196349
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362007, nssv14362008
SamplesNA19240, HG00514
Known GenesTESK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232659
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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