A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706338



Internal ID21228132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18881549..18881602hg38UCSC Ensembl
chrX:18899667..18899720hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706338
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.40625


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