A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872839



Internal ID22647781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:96892137..97019082hg38UCSC Ensembl
chrX:96147136..96274081hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38126946
hg19126946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451060
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872839
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