A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106850



Internal ID22016083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50723171..50723282hg38UCSC Ensembl
chrX:50466171..50466282hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645575
Samples
Known GenesSHROOM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106850
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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