A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570744



Internal ID21762787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40491508..40491699hg38UCSC Ensembl
chr6:40459247..40459438hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003726
Supporting Variants
Samples
Known GenesLRFN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570744
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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