A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137966



Internal ID337147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16801362..16809525hg38UCSC Ensembl
chrX:16819485..16827648hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg388164
hg198164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739452
Samples
Known GenesTXLNG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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