A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094924



Internal ID22004157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58621956..58621956hg38UCSC Ensembl
chr10:60381716..60381716hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587031
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094924
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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