A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284647



Internal ID20493865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124334363..124334546hg38UCSC Ensembl
chrX:123468213..123468396hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284647
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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