A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351832



Internal ID22231991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57169496..57169560hg38UCSC Ensembl
chrX:57195929..57195993hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525336
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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