A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516004



Internal ID22573966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23820704..23830094hg38UCSC Ensembl
chrX:23838821..23848211hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg389391
hg199391
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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