A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455138



Internal ID22513015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3267820..3269936hg38UCSC Ensembl
chrX:3185861..3187977hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382117
hg192117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880125
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455138
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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