A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091761



Internal ID22000994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78468548..78468548hg38UCSC Ensembl
chr10:80228305..80228305hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091761
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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