A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587629



Internal ID20960700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54095245..54096518hg38UCSC Ensembl
chr18:51621615..51622888hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3371n223
Supporting Variantsnssv18244673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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