A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540746



Internal ID20914036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226171733..226172254hg38UCSC Ensembl
chr2:227036449..227036970hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257177
Samples
Known GenesLOC646736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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