A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979470



Internal ID22754405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3093681..3109071hg38UCSC Ensembl
chrX:3011722..3027112hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3815391
hg1915391
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516132
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979470
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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