A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968612



Internal ID22743547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115683697..115688945hg38UCSC Ensembl
chrX:114918017..114923265hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385249
hg195249
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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