A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072084



Internal ID21981317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37036890..37036890hg38UCSC Ensembl
chr4:37038512..37038512hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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