A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979663



Internal ID22754598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42653025..42654593hg38UCSC Ensembl
chrX:42512277..42513845hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381569
hg191569
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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