A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545597



Internal ID20918828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230970229..230970741hg38UCSC Ensembl
chr2:231834944..231835456hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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