A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561302



Internal ID21885657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25586424..25586535hg38UCSC Ensembl
chr6:25586652..25586763hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005737
Supporting Variants
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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