A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967802



Internal ID22742738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22477266..22507868hg38UCSC Ensembl
chrX:22495383..22525985hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3830603
hg1930603
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515979
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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