A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046941



Internal ID21956175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151373624..151373624hg38UCSC Ensembl
chrX:150542096..150542096hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046941
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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