A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975903



Internal ID22750838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152465883..152476829hg38UCSC Ensembl
chrX:151634355..151645301hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810947
hg1910947
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975903
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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