A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979254



Internal ID22754189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56461547..56491397hg38UCSC Ensembl
chrX:56487980..56517830hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3829851
hg1929851
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516407, nssv17516406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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