A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516861



Internal ID22574824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84191944..84198343hg38UCSC Ensembl
chrX:83446952..83453351hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516861
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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