A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880215



Internal ID22655185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142766781..142772347hg38UCSC Ensembl
chrX:141854567..141860133hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg385567
hg195567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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