A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402194



Internal ID21059747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64054342..64110696hg38UCSC Ensembl
chr6:64764235..64820589hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3856355
hg1956355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143012
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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