A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045902



Internal ID21955160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140689788..140689788hg38UCSC Ensembl
chrX:139771953..139771953hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045902
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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