A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077978



Internal ID21987211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43088145..43088145hg38UCSC Ensembl
chr5:43088247..43088247hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556826
Samples
Known GenesLOC100506639
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077978
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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