A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055876



Internal ID21965109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17696145..17696145hg38UCSC Ensembl
chrX:17714265..17714265hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638142
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055876
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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