A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091949



Internal ID22001182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123904891..123904891hg38UCSC Ensembl
chr10:125664407..125664407hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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