A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074742



Internal ID21983975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175420606..175420606hg38UCSC Ensembl
chr5:174847609..174847609hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074742
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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