A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326740



Internal ID20859877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89054147..89087272hg38UCSC Ensembl
chr1:89519830..89552955hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3833126
hg1933126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205213
Samples
Known GenesGBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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