A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102029



Internal ID22011262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1563126..1563199hg38UCSC Ensembl
chrX:1682019..1682092hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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