A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550029



Internal ID20923181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62154518..62155718hg38UCSC Ensembl
chr2:62381653..62382853hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3903n223
Supporting Variantsnssv18260833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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