A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976290



Internal ID22751225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:117870755..117895845hg38UCSC Ensembl
chrX:117004718..117029808hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3825091
hg1925091
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976290
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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