A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576495



Internal ID20949566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31953803..31955505hg38UCSC Ensembl
chr18:29533766..29535468hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381703
hg191703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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