A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14298676



Internal ID22185897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10415675..10421414hg38UCSC Ensembl
chr20:10396323..10402062hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg385740
hg195740
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3235744
Supporting Variants
SamplesHG00731
Known GenesMKKS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14298676
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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