A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354889



Internal ID22141490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153542049..153542120hg38UCSC Ensembl
chrX:152807507..152807578hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194982
Supporting Variants
SamplesHG00513
Known GenesATP2B3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354889
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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