A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548176



Internal ID20921372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30062695..30097071hg38UCSC Ensembl
chr2:30285561..30319937hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3834377
hg1934377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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