A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104077



Internal ID22013311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30232707..30233136hg38UCSC Ensembl
chrX:30250824..30251253hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642898
Samples
Known GenesMAGEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104077
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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