A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423855



Internal ID21081408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63176297..63182005hg38UCSC Ensembl
chr8:64088856..64094564hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg385709
hg195709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169798
Samples
Known GenesYTHDF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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