A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644794



Internal ID21836841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54788593..54788593hg38UCSC Ensembl
chrX:54815026..54815026hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042955
Supporting Variants
Samples
Known GenesITIH6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644794
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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