A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546319



Internal ID20919537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218497375..218498545hg38UCSC Ensembl
chr2:219362098..219363268hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259342
Samples
Known GenesUSP37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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