A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885592



Internal ID22660576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21677303..21677376hg38UCSC Ensembl
chrX:21695421..21695494hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885592
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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