A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883559



Internal ID22658540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2952216..2952314hg38UCSC Ensembl
chrX:2870257..2870355hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454494
Samples
Known GenesARSE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883559
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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