A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006304



Internal ID21915647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64330123..64344863hg38UCSC Ensembl
chr6:65040016..65054756hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3814741
hg1914741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563578
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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