A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535686



Internal ID20909040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230522788..230524350hg38UCSC Ensembl
chr2:231387503..231389065hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257294
Samples
Known GenesSP100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535686
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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