A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533439



Internal ID20906800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5929301..5934500hg38UCSC Ensembl
chr18:5929300..5934499hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3272n223
Supporting Variantsnssv18042375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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