A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068381



Internal ID21977614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173799112..173799112hg38UCSC Ensembl
chr4:174720263..174720263hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068381
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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