A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565651



Internal ID21757616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25031729..25031783hg38UCSC Ensembl
chr6:25031957..25032011hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015558
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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