A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450624



Internal ID22508496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86834564..86835430hg38UCSC Ensembl
chrX:86089567..86090433hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450624
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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