A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072075



Internal ID21981308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88930080..88930080hg38UCSC Ensembl
chr6:89639799..89639799hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568176
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072075
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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