A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554409



Internal ID20927505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60758602..60759250hg38UCSC Ensembl
chr2:60985737..60986385hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3896n223
Supporting Variantsnssv18257663
Samples
Known GenesPAPOLG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554409
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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