A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097445



Internal ID22006678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63870615..63870615hg38UCSC Ensembl
chr10:65630375..65630375hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097445
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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