A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880716



Internal ID22655686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75334611..75334803hg38UCSC Ensembl
chrX:74554446..74554638hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880716
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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