A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294818



Internal ID20504036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142351637..142351702hg38UCSC Ensembl
chrX:141439423..141439488hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294818
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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