A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880090



Internal ID22655060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84743719..84743785hg38UCSC Ensembl
chrX:83998727..83998793hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880090
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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