A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092574



Internal ID22001807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72326427..72326427hg38UCSC Ensembl
chr10:74086185..74086185hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092574
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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