A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328113



Internal ID20861258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45416889..45417341hg38UCSC Ensembl
chr1:45882561..45883013hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061083
Samples
Known GenesTESK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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