A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106904



Internal ID22016137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101515300..101515480hg38UCSC Ensembl
chrX:100770287..100770467hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638706
Samples
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106904
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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