A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455011



Internal ID22512888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3195878..3205312hg38UCSC Ensembl
chrX:3113919..3123353hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389435
hg199435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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