A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977462



Internal ID22752397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54915317..54920606hg38UCSC Ensembl
chrX:54941750..54947039hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg385290
hg195290
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516381
Samples
Known GenesTRO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977462
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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