A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101909



Internal ID22011142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54434153..54445835hg38UCSC Ensembl
chrX:54460586..54472268hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3811683
hg1911683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639576
Samples
Known GenesFGD1, TSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101909
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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