A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076991



Internal ID21986224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110473739..110473739hg38UCSC Ensembl
chr6:110794942..110794942hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563737
Samples
Known GenesSLC22A16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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