A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969683



Internal ID22744618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3784260..3797213hg38UCSC Ensembl
chrX:3702301..3715254hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3812954
hg1912954
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969683
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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