A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044412



Internal ID21953694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62841230..62841230hg38UCSC Ensembl
chrX:62060700..62060700hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044412
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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