A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280427



Internal ID20489645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128773939..128774037hg38UCSC Ensembl
chrX:127907917..127908015hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280427
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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