A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638111



Internal ID21830158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35301149..35301149hg38UCSC Ensembl
chrX:35319266..35319266hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg381924
hg191924
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638111
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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