A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968638



Internal ID22743573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2358321..2375335hg38UCSC Ensembl
chrX:2276362..2293376hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3817015
hg1917015
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515993
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968638
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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