A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351101



Internal ID22263382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46498861..46499236hg38UCSC Ensembl
chrX:46358296..46358671hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200243
Supporting Variants
SamplesNA19238
Known GenesZNF674
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351101
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