A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763856



Internal ID20539716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112241126..112241126hg38UCSC Ensembl
chr6:112562327..112562327hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285643
Samples
Known GenesLAMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763856
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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