A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351580



Internal ID22194395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9716773..9721703hg38UCSC Ensembl
chrX:9684813..9689743hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230550
Supporting Variants
SamplesHG00731
Known GenesTBL1X
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351580
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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