A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110989



Internal ID22020222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137206122..137208300hg38UCSC Ensembl
chrX:136288281..136290459hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg382179
hg192179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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