A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041749



Internal ID21951079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81362340..81362340hg38UCSC Ensembl
chrX:80617839..80617839hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041749
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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