A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546632



Internal ID20919842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143053434..143056344hg38UCSC Ensembl
chr2:143811003..143813913hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg382911
hg192911
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4145n223
Supporting Variantsnssv18253865
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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