A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516322



Internal ID22574284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51099419..51103756hg38UCSC Ensembl
chrX:50842265..50846602hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg384338
hg194338
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516322
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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