A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647638



Internal ID21839685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17901920..17901920hg38UCSC Ensembl
chrX:17920040..17920040hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647638
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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