A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101283



Internal ID22010516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155803823..155983788hg38UCSC Ensembl
chrX:155033486..155213453hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38179966
hg19179968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648411
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101283
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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