A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516193



Internal ID22574155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37064883..37079013hg38UCSC Ensembl
chrX:37082956..37097086hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3814131
hg1914131
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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