A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818866



Internal ID21264204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25929824..25930157hg38UCSC Ensembl
chrX:25947941..25948274hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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