A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301861



Internal ID22186851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32427859..32433796hg38UCSC Ensembl
chr21:33800167..33806104hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385938
hg195938
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212930
Supporting Variants
SamplesHG00731
Known GenesEVA1C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301861
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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