A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637548



Internal ID21829595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153747407..153748718hg38UCSC Ensembl
chrX:153012861..153014172hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637548
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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