A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595253



Internal ID20968324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4642259..4649019hg38UCSC Ensembl
chr18:4642260..4649020hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386761
hg196761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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