A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210060



Internal ID22358040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32320769..32323177hg38UCSC Ensembl
chr1:32786370..32788778hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359270
SamplesHG00513
Known GenesHDAC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210060
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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