A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540659



Internal ID20913948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32261330..32262087hg38UCSC Ensembl
chr2:32486399..32487156hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260073
Samples
Known GenesNLRC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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