A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086355



Internal ID21995588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6480681..6480681hg38UCSC Ensembl
chr12:6589847..6589847hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086355
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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