A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301663



Internal ID22140679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44697551..44709800hg38UCSC Ensembl
chr21:46117466..46129715hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812250
hg1912250
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215002
Supporting Variants
SamplesHG00513
Known GenesKRTAP10-12, TSPEAR
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301663
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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