A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458215



Internal ID22516096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92840164..92840393hg38UCSC Ensembl
chrX:92095163..92095392hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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