A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106580



Internal ID22015813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151808685..151809052hg38UCSC Ensembl
chrX:150977157..150977524hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106580
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