A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552218



Internal ID20925346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14782375..14797735hg38UCSC Ensembl
chr2:14922499..14937859hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3815361
hg1915361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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