A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351837



Internal ID22322045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57608942..57609000hg38UCSC Ensembl
chrX:57635375..57635433hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190840
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351837
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