A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041475



Internal ID21950808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70468923..70468923hg38UCSC Ensembl
chrX:69688773..69688773hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649505
Samples
Known GenesDLG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041475
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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