A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548767



Internal ID20921949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200893898..200894402hg38UCSC Ensembl
chr2:201758621..201759125hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256359
Samples
Known GenesNIF3L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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