A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544795



Internal ID20918032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62338800..62339325hg38UCSC Ensembl
chr2:62565935..62566460hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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