A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350982



Internal ID22156204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3387569..3387821hg38UCSC Ensembl
chrX:3305610..3305862hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198049
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350982
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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