A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649162



Internal ID21841209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130193209..130193287hg38UCSC Ensembl
chrX:129327183..129327261hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649162
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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