A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334765



Internal ID20867953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66893201..66894400hg38UCSC Ensembl
chr1:67358884..67360083hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062637
Samples
Known GenesWDR78
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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