A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873708



Internal ID22648656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62769084..62780631hg38UCSC Ensembl
chrX:61988554..62000101hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3811548
hg1911548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873708
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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