A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072217



Internal ID21981450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7979439..7979439hg38UCSC Ensembl
chr4:7981166..7981166hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547395
Samples
Known GenesABLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072217
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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