A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291231



Internal ID20500449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166396244..166396328hg38UCSC Ensembl
chr6:166809732..166809816hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291231
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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