A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551243



Internal ID20924380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36953969..36954684hg38UCSC Ensembl
chr2:37181112..37181827hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260170
Samples
Known GenesSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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