A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880423



Internal ID22655393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27188379..27190136hg38UCSC Ensembl
chrX:27206496..27208253hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880423
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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