A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299758



Internal ID22223693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62971488..62971545hg38UCSC Ensembl
chr20:61602840..61602897hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219582
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299758
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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