A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066149



Internal ID21975382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81750698..81750698hg38UCSC Ensembl
chr3:81799849..81799849hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555891
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066149
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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