A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351561



Internal ID22139438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7622684..7622854hg38UCSC Ensembl
chrX:7540725..7540895hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558498
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351561
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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