A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107475



Internal ID22016708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50795101..50795160hg38UCSC Ensembl
chrX:50538101..50538160hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645730
Samples
Known GenesSHROOM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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