A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072127



Internal ID21981360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84214796..84214796hg38UCSC Ensembl
chr6:84924514..84924514hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577071
Samples
Known GenesKIAA1009
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072127
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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