A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433261



Internal ID22491131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133443435..133443495hg38UCSC Ensembl
chrX:132577463..132577523hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433261
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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