A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399850



Internal ID21057403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64508873..64540519hg38UCSC Ensembl
chr6:65218766..65250412hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3831647
hg1931647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219265
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399850
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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