A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968196



Internal ID22743131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35854740..35871605hg38UCSC Ensembl
chrX:35872857..35889722hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3816866
hg1916866
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968196
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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