A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819777



Internal ID21265115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123260512..123260512hg38UCSC Ensembl
chrX:122394363..122394363hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711660
Samples
Known GenesGRIA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819777
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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