A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049941



Internal ID21959174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135012913..135012913hg38UCSC Ensembl
chrX:134146943..134146943hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049941
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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