A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968772



Internal ID22743707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155636232..155640598hg38UCSC Ensembl
chrX:154865893..154870259hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384367
hg194367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968772
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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