A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351104



Internal ID22263389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46935144..46936222hg38UCSC Ensembl
chrX:46794579..46795657hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525549
Supporting Variants
SamplesNA19238
Known GenesJADE3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351104
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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