A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105850



Internal ID22015083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129989278..129990369hg38UCSC Ensembl
chrX:129123254..129124345hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg381092
hg191092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105850
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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