A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070406



Internal ID21979639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178985440..178985440hg38UCSC Ensembl
chr5:178412441..178412441hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567156
Samples
Known GenesGRM6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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