A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108582



Internal ID22017815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130173667..130178781hg38UCSC Ensembl
chrX:129307641..129312755hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg385115
hg195115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641930
Samples
Known GenesRAB33A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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