A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056891



Internal ID21966126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100917656..100917656hg38UCSC Ensembl
chrX:100172645..100172645hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640163
Samples
Known GenesXKRX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056891
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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