A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286216



Internal ID20495434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3072439..3072633hg38UCSC Ensembl
chrX:2990480..2990674hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752075
Supporting Variants
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286216
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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