A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412336



Internal ID21069889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63929416..63929837hg38UCSC Ensembl
chr6:64639309..64639730hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143002
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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