A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351805



Internal ID22321981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55930790..55930846hg38UCSC Ensembl
chrX:55957223..55957279hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526667
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351805
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer