A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072885



Internal ID21982118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3377501..3377501hg38UCSC Ensembl
chr5:3377615..3377615hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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