A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754112



Internal ID20529972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54434153..54445836hg38UCSC Ensembl
chrX:54460586..54472269hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3811684
hg1911684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287246
Samples
Known GenesFGD1, TSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754112
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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