A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045975



Internal ID21955227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30310831..30310831hg38UCSC Ensembl
chrX:30328948..30328948hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045975
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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