A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075806



Internal ID21985039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75927807..75927807hg38UCSC Ensembl
chr6:76637524..76637524hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577152
Samples
Known GenesIMPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075806
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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