A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967916



Internal ID22742851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151489182..151490419hg38UCSC Ensembl
chrX:150657654..150658891hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515628, nssv17515629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967916
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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