A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978330



Internal ID22753265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153293293..153301173hg38UCSC Ensembl
chrX:152558751..152566631hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387881
hg197881
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515678, nssv17515679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978330
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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