A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752702



Internal ID20528562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27809434..27809488hg38UCSC Ensembl
chrX:27827551..27827605hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279207
Samples
Known GenesMAGEB10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752702
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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