A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105220



Internal ID22014453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17911768..17911822hg38UCSC Ensembl
chrX:17929888..17929942hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105220
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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