A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299852



Internal ID22186227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739564..32740227hg38UCSC Ensembl
chr20:31327371..31328034hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219954
Supporting Variants
SamplesHG00731
Known GenesCOMMD7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299852
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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