A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003409



Internal ID21912752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65529376..65529428hg38UCSC Ensembl
chr8:66441611..66441663hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590815
Samples
Known GenesLOC286186
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003409
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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