A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102207



Internal ID22011442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124904836..124905903hg38UCSC Ensembl
chrX:124038685..124039752hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649657
Samples
Known GenesTENM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102207
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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