A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752075



Internal ID20527935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3072439..3072633hg38UCSC Ensembl
chrX:2990480..2990674hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286216
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752075
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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