A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451283



Internal ID22509155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90038371..90038472hg38UCSC Ensembl
chrX:89293370..89293471hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451283
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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