A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549089



Internal ID20922260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70755952..70756920hg38UCSC Ensembl
chr2:70983084..70984052hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3921n223
Supporting Variantsnssv18258945
Samples
Known GenesADD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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