A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090213



Internal ID21999446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92861157..92861157hg38UCSC Ensembl
chr12:93254933..93254933hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611823
Samples
Known GenesEEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090213
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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