A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285643



Internal ID20494861
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 StatusS
Merged Variantsnsv4763856
Supporting Variants
Samples
Known GenesLAMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285643
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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