A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872296



Internal ID22647235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80214998..80215110hg38UCSC Ensembl
chrX:79470497..79470609hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872296
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