A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876266



Internal ID22651226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31137680..31139687hg38UCSC Ensembl
chrX:31155797..31157804hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461153
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876266
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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