A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332330



Internal ID20865500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45417843..45419228hg38UCSC Ensembl
chr1:45883515..45884900hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381386
hg191386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061085
Samples
Known GenesTESK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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