A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046251



Internal ID21955496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42742098..42742098hg38UCSC Ensembl
chrX:42601349..42601349hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046251
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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