A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974236



Internal ID22749171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21338849..21343208hg38UCSC Ensembl
chrX:21356967..21361326hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg384360
hg194360
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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