A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093715



Internal ID22002948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69992870..69992870hg38UCSC Ensembl
chr10:71752626..71752626hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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