A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641955



Internal ID21834002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151718145..151718200hg38UCSC Ensembl
chrX:150886617..150886672hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103248
Supporting Variants
Samples
Known GenesFATE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641955
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