A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736197



Internal ID20512144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111903221..111908454hg38UCSC Ensembl
chr6:112224424..112229657hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736197
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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