A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271060



Internal ID20480278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64785087..64842355hg38UCSC Ensembl
chrX:64004967..64062235hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3857269
hg1957269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271060
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