A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538674



Internal ID20911988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25436064..25437550hg38UCSC Ensembl
chr2:25658933..25660419hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381487
hg191487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258149
Samples
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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