A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879642



Internal ID22654613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28285302..28286701hg38UCSC Ensembl
chrX:28303419..28304818hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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