A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093585



Internal ID22002818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:72507..72507hg38UCSC Ensembl
chr12:181673..181673hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607393
Samples
Known GenesIQSEC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093585
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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