A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076039



Internal ID21985272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157350882..157350882hg38UCSC Ensembl
chr6:157771914..157771914hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076039
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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