A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976518



Internal ID22751453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:91330251..91338103hg38UCSC Ensembl
chrX:90585250..90593102hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg387853
hg197853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976518
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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