A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818891



Internal ID21264229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29802914..29802914hg38UCSC Ensembl
chrX:29821031..29821031hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709825
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818891
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