A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074718



Internal ID21983951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186015112..186015112hg38UCSC Ensembl
chr3:185732901..185732901hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074718
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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