A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110696



Internal ID22019929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103021766..103021826hg38UCSC Ensembl
chrX:102276694..102276754hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110696
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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