A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818809



Internal ID21264147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14899115..14899115hg38UCSC Ensembl
chrX:14917237..14917237hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698358
Samples
Known GenesMOSPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818809
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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