A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277291



Internal ID20486509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18201521..18201614hg38UCSC Ensembl
chrX:18219641..18219734hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758882
Supporting Variants
Samples
Known GenesBEND2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277291
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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