A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353386



Internal ID22266025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143750269..143750392hg38UCSC Ensembl
chrX:142833364..142833487hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526330
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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