A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070880



Internal ID21980113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:45373856..45373856hg38UCSC Ensembl
chr5:45373958..45373958hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549897
Samples
Known GenesHCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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