A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071000



Internal ID21980233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76776534..76776534hg38UCSC Ensembl
chr8:77688770..77688770hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589615
Samples
Known GenesZFHX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071000
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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