A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327880



Internal ID20861024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63289318..63290282hg38UCSC Ensembl
chr1:63754989..63755953hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062276
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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