A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466165



Internal ID22524054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5281418..5281479hg38UCSC Ensembl
chrX:5199459..5199520hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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