A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075973



Internal ID21985206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17041198..17041198hg38UCSC Ensembl
chr6:17041429..17041429hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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