A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756769



Internal ID20532629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77036099..77036099hg38UCSC Ensembl
chr8:77948335..77948335hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756769
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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