A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042873



Internal ID21952185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30233032..30233032hg38UCSC Ensembl
chrX:30251149..30251149hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637894
Samples
Known GenesMAGEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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