A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454588



Internal ID22512464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67198196..67198429hg38UCSC Ensembl
chrX:66418038..66418271hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454588
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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