A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820481



Internal ID21265819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3326186..3326186hg38UCSC Ensembl
chrX:3244227..3244227hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705823, nssv13707511
Samples
Known GenesMXRA5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820481
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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