A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756881



Internal ID20532741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85767564..85767564hg38UCSC Ensembl
chr2:85994687..85994687hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283085
Samples
Known GenesATOH8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756881
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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