A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756239



Internal ID20532099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126158245..126158245hg38UCSC Ensembl
chr10:127846814..127846814hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285562
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756239
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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